Seizure Semiology ILAE
Seizure Semiology ILAE
Seizure Semiology ILAE
1
Department of Clinical
Neurophysiology, Aarhus University
Hospital, Aarhus, Denmark
2
Danish Epilepsy Centre, Dianalund,
Seizure semiology: ILAE
Denmark
3
4
Department of Clinical Medicine,
Aarhus University, Aarhus Denmark
Department of Neurology, Mayo
glossary of terms and their
Clinic, Jacksonville, FL, USA
5
Departments of Neurology,
Neuroscience, Neurosurgery, Yale
University School of Medicine, New
significance
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
Correspondence:
Sándor Beniczky witnessed seizures [1], more detailed ings) are essential for correct
Aarhus University Hospital feature-extraction is possible by review- characterization of the seizures, and
and Danish Epilepsy Center, ing video recordings of the typical for correct localization and lateraliza-
Visby Allé 5, 4293, events [2]. Recent technological tion, as described in detail in a previous
Dianalund, Denmark
advances with high-resolution video seminar in epileptology [1]. The term
<sbz@filadelfia.dk>
<[email protected]> cameras allow recording of subtle aura denotes subjective symptoms at
seizure onset that are perceived by the patient. It has 1. Electrographic seizures
been described in focal seizures (i.e., focal aware
seizures and at the onset of focal impaired awareness Electrographic seizures are subclinical and do not
seizures, before impairment of consciousness). Aura have any observable signs or reported symptoms
has also been reported in generalized seizures. despite an unequivocal ictal pattern on EEG:
Epileptic aura must be differentiated from aura 1) sustained spike-wave discharges with a frequency
occurring in non-epileptic paroxysmal events (mi- 2.5 Hz; 2) rhythmic – evolving ictal activity (with a
graine, syncope, dissociative seizures). dynamic evolution in time and space). Electrographic
Our goal is to provide a list of terms that are used to seizures (10 seconds and longer) and electrographic
describe seizure semiology, and to update the status epilepticus (10 minutes and longer) are often
glossary initially developed in the ILAE Commission recorded in critically ill patients [9-12], and also in
report published 20 years ago [3]. Semiology features genetic or developmental / epileptic encephalopa-
were subdivided to reflect similar signs and their
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
~
Table 1. Key points showing the most accepted localization and lateralization signs for the most important
semiological features.
Body-perception T, P, O
illusion
Depersonalization
Forced thinking
Gustatory Ins Posterior-dorsal part
Olfactory T, F, Ins Amygdala, orbito-
Sensory frontal cortex,
phenomena posterio-dorsal insula
Non painful CON When unilateral P Sensory cortex (S1)
Somatosensory Painful & CON When unilateral Ins Posterior-superior
thermal insula
Vestibular T, P Posterior temporo-
perisylvian cortex,
including insula
Visual CON When unilateral, O Visual cortex (V1)
mainly elementary
hallucinations
Anger T, F Amygdala, prefrontal
(orbito-frontal)
Anxiety T Amygdala
Ecstatic/bliss Ins Anterior dorsal Insula
Fear T, F Amygdala, orbito-
Affective frontal cortex, anterior
(emotional) cingulate
phenomena Guilt
Mirth
Mystic T
Sadness
Sexual
Aphasia T, P, F Broca, Wernicke, basal
temporal language area
Cognitive
phenomena Dysmnesia
Dysmnesia Amnesia
~
Table 1. Key points showing the most accepted localization and lateralization signs for the most important
semiological features (continued).
~
Table 1. Key points showing the most accepted localization and lateralization signs for the most important
semiological features (continued).
dacrystic
Oro-alimentary ND When awareness is
automatisms preserved
Verbal T Related to insulo-
automatisms opercular involvement
Vocal D In context of TLE and
automatisms FLE
Hyperkinetic
behaviour
Bradycardia + T, F Bilateral temporal,
ictal asystole orbito-frontal
Cardiovascular
Tachycardia T
Flushing
Pallor
Cutaneous
Piloerection
Sweating
Epigastric T Mainly when followed
by automatisms
Flatulence
~
Table 1. Key points showing the most accepted localization and lateralization signs for the most important
semiological features (continued).
dysfunction
Postictal Postictal nose- IPSI In the context of TLE T, F Temporal more than
phenomena wiping frontal
Postictal
pallinacousis
Postictal paresis CON
(Todd’s paresis)
Postictal
psychiatric signs
Postictal
unresponsiveness
D: dominant; ND: non-dominant; CON: contralateral; IPSI: ipsilateral; TLE: temporal lobe epilepsy; FLE: frontal lobe epilepsy; F: frontal; T: temporal;
P: parietal; O: occipital, Ins: insula; Operc: opercular; Ins: insula; Hypoth: hypothalamus.
awareness for events occurring during the seizure was sies, impaired awareness may be more common in
retained or impaired”. However, the postictal recall is dominant hemispheric onset [29, 42, 43], although
also affected by the ictal involvement of language and this could be biased by mainly verbal tests used for
memory, not only awareness per se. Even with these assessment. In most of the temporal lobe epilepsies,
limitations, awareness is used as a core descriptor to the awareness becomes impaired when the seizure
stratify focal seizures in the recent ILAE classification involves neocortical and subcortical structures
of seizures [5]. Patient awareness about the occur- [25, 29].
rence of a seizure is another completely different
attribute, which might be clinically relevant for 2.2. Responsiveness
planning diagnostic and management strategies [31].
Impaired awareness (inability of the person having the Responsiveness during the seizure to questions,
seizure to later verify retained awareness) occurs in commands or other stimuli is used as a descriptor,
generalized or bilateral tonic-clonic seizures with but not as a classifier, because “some people are
uncommon exceptions [23, 32-34]. Most absence immobilized and consequently unresponsive during a
seizures cause impaired awareness [20-23]. However, seizure, but still able to observe and recall their
in some cases during bursts of generalized spike-wave environment” [5]. Despite not being used as a
discharges, the patient does not follow commands classifier, responsiveness during seizures is highly
and is unable to repeat the test words (impaired clinically relevant, for example in evaluating driving
responsiveness), yet after the spike-wave bursts safety [5, 17, 44-46]. Responsiveness is used as a
terminate, the patient is able to recall the commands standard means of assessment in other neurological
and test words given during the seizure, demonstrat- disorders of consciousness [47-49], and is commonly
ing retained awareness during the electroclinical used in epilepsy monitoring units because it is
absence seizure (non-responsive patient with ictal relatively objective and does not rely on patient
EEG correlate) [21, 22, 35-41]. In temporal lobe epilep- subjective report. Testing batteries should be used for
~
Table 2. Seizure semiology: videos.
~
Table 2. Seizure semiology: videos (continued).
~
Table 2. Seizure semiology: videos (continued).
~
Table 2. Seizure semiology: videos (continued).
in IGE) with_tonicclonic_seizures__261669/article.
last jerks on the R ! stridor phtml?tab=videos&cle_video_une=285336
[412]
b. Tonic-clonic Ictal cry ! Bilateral tonic symmetric ! Bilateral Supplementary video 7
(GTCS in IGE) tonic-clonic symmetric Supplementary figure 6A, B
(Note the surface EMG channels showing the
gradual “build up” of the muscle artifact during
the tonic phase, followed by gradually longer
“silent” periods corresponding to the clonic
phase of a GTCS)
Aura ! R head version ! tonic ! figure-of- https://www.jle.com/en/revues/epd/e-
four ! bilat tonic-clonic ! postictal docs/classification_of_paroxysmal_events_and_
unresponsiveness the_four_dimensional_epilepsy_classification_
system_313798/article.phtml?tab=videos&cle_
video_une=313811
Figure-of-four [410]
(FBTCS)
Refer to dystonic and asymmetric clonic https://www.jle.com/en/revues/epd/e-
termination docs/video_atlas_of_lateralising_and_localising_
seizure_phenomena_288739/article.phtml?tab=
videos&cle_video_une=289022
[403]
Refer to tonic-clonic (GTCS with lateralizing https://www.jle.com/en/revues/epd/e-
features in IGE) docs/videoeeg_evidence_of_lateralized_clinical_
features_in_primary_generalized_epilepsy_
with_tonicclonic_seizures__261669/article.
phtml?tab=videos&cle_video_une=285336
Asymmetric clonic [412]
ending
Refer to dystonic and figure-of-four https://www.jle.com/en/revues/epd/e-
docs/video_atlas_of_lateralising_and_localising_
seizure_phenomena_288739/article.phtml?tab=
videos&cle_video_une=289022
[403]
Versive Upward eye deviation ! R eye and head https://www.jle.com/en/revues/epd/e-
version ! R Tonic arm flexion ! clonic jerks docs/adversive_seizures_associated_with_
in R side of face and R arm periodic_lateralised_epileptiform_discharges_
pleds_after_left_orbital_contusion_
294991/article.phtml?tab=videos&cle_video_
une=295286
[418]
~
Table 2. Seizure semiology: videos (continued).
~
Table 2. Seizure semiology: videos (continued).
~
Table 2. Seizure semiology: videos (continued).
[431]
AFFECTIVE (EMOTIONAL) PHENOMENA
Anger S1: R gestural + oroalimentary automatisms ! https://www.jle.com/en/revues/epd/e-
ictal speech + affective (anger) ! ictal docs/seizure_semiology_of_anti_lgi1_antibody_
vocalization. S2: L face grimacing ! non-fluent encephalitis_310814/article.phtml?tab=videos&
aphasia (anomia) cle_video_une=311024
S3: R gestural automatisms ! affective [425]
S4: R gestural automatisms ! ictal speech +
affective (anger)
Anxiety Anxiety + hyperventilation ! L somatosensory https://www.jle.com/en/revues/epd/e-docs/long_
aura! vestibular symptoms ! dysarthria ! lasting_seizure_related_anxiety_in_patients_
ictal cry with_temporal_lobe_epilepsy_and_comorbid_
psychiatric_disorders_305196/article.phtml?tab=
videos&cle_video_une=305316
[432]
Ictal fear + ictal vocalization ! L head version https://www.jle.com/en/revues/epd/e-
+ dystonic posture ! L hand automatisms + docs/semiological_study_of_ictal_affective_
non-responsive behaviour_in_epilepsy_and_mental_retardation_
limited_to_females_efmr__293200/article.phtml?
tab=videos&cle_video_une=295278
Fear
[433]
Focal impaired awareness seizure: ictal fear ! Supplementary video 8
hyperkinetic behavior Supplementary figure 7
(See Hyperkinetic)
Mystic S1: verbal automatisms (repeating religious https://www.jle.com/en/revues/epd/e-docs/ictal_
statement) ! ictal kissing ! L gestural kissing_and_religious_speech_in_a_patient_
automatisms ! oroalimentary automatisms with_right_temporal_lobe_epilepsy__
S2: hyperventilation ! Bilateral gestural 265692/article.phtml?tab=videos&cle_video_
automatisms ! verbal automatisms (repeating une=285267
religious passages) ! musical automatism [424]
(whistling) + Bilateral gestural automatisms !
ictal kissing ! oroalimentary automatisms ! L
gestural automatisms ! oroalimentary ! R
gestural automatisms ! non-responsive
COGNITIVE PHENOMENA
Focal impaired awareness seizure: R gestural Supplementary video 9
automatisms ! ictal aphasia Supplementary figure 8
Epigastric aura (presses the alarm button) https://www.jle.com/en/revues/epd/e-
Aphasia !responsive (follows command to raise R arm) docs/video_atlas_of_lateralising_and_localising_
! ictal aphasia/anomia (unable to name seizure_phenomena_288739/article.phtml?tab=
objects)+ R hand ictal dystonia videos&cle_video_une=289023
[403]
~
Table 2. Seizure semiology: videos (continued).
~
Table 2. Seizure semiology: videos (continued).
williams_syndrome_313319/article.phtml?tab=
videos&cle_video_une=313364
[434]
POSTICTAL PHENOMENA
Postictal nose wiping (Seizure from sleep) opening eyes ! https://www.jle.com/en/revues/epd/e-
oroalimentary automatisms ! R gestural docs/seizure_ending_signs_in_patients_with_
automatisms ! responsive ! R postictal nose dyscognitive_focal_seizures_305235/article.
wiping phtml?tab=videos&cle_video_une=305312
(see Distal Automatisms) [419]
Postictal paresis and Ictal: L head version ! L gestural automatisms https://www.jle.com/en/revues/epd/e-
aphasia ! R gestural automatisms + R arm dystook nic. docs/postictal_signs_of_lateralizing_and_
Postictal: L nose wiping, R (Todd’s) paresis, and localizing_significance_published_with_
non-fluent aphasia. videosequences_._110069/article.phtml?tab=
(Sequence 1, up to Section 5.05) videos&cle_video_une=285233
(see also under Dystonic and Distal [374]
Automatisms)
Postictal coughing, Oroalimentary automatisms ! Bilateral leg https://www.jle.com/en/revues/epd/e-
nose wiping and proximal automatisms ! hyperventilation ! docs/autonomic_symptoms_during_epileptic_
unresponsiveness vocal automatisms +R arm dystonic ! seizures_110095/article.phtml?tab=videos&cle_
nonresponsive L arm gestural automatisms ! L video_une=285222
arm exploratory movements ! Postictal: L nose [295]
wiping + coughing, + unresponsiveness
standardized behavioral testing of the patients in ate responses and/or an unusually prolonged reaction
epilepsy monitoring units [18]. An appropriate re- time.
sponse is a composite end-result of functional Responsiveness is lost in generalized tonic-clonic
activities in complex neurological networks, which seizures (GTCS), but not necessarily during general-
might include proper sensory perception and proces- ized myoclonic seizures. In most absence seizures,
sing along with prompt motor execution. These patients are non-responsive, but the responsiveness
responses might be context and culture specific, might be partial [21, 22, 40]. In focal seizures, partial or
affected by the intellectual and emotional level of the complete absence of responsiveness might be seen.
patient [19, 24]. Verbal responses might be more affected in focal
Non-responsive implies lack of response to repeated epilepsies with dominant hemispheric involvement,
questions commands or other external stimuli. Spinal while partial responsiveness during automatisms
reflex withdrawal in response to a noxious stimulus suggests involvement of the non-dominant hemi-
without an appropriate emotional response might still sphere [20, 50, 51].
occur in this non-responsive phase [14, 19, 23]. Motor or behavioral arrest is related but not identical
Partially responsive implies inconsistent, inappropri- to impaired responsiveness. Behavioral arrest is
common in absence seizures and in focal seizures leads to falling without specificity for identifying the
with impaired awareness or impaired responsiveness. underlying mechanism (i.e., from atonic, myoclonic,
However, behavioral arrest may be observed based on or tonic seizures) which is most often ill-defined in the
interruption of ongoing motor activity even if absence of polygraphic video-EEG monitoring that
responsiveness to external stimuli is not assessed. involves recording surface electromyography.
3.3. Atonic
3. Elementary motor signs
Atonic refers to a sudden loss or decrease in muscle
Elementary or simple motor signs involve the skeletal tone involving the head, trunk, jaw, and limbs. Atonic
musculature during seizures. They consist of an seizures typically last 1-2 seconds and can result
increase (positive) or decrease (negative) in contrac- in a loss of postural tone, without tonic, clonic,
tion of a muscle or group of muscles that is unnatural, or myoclonic manifestations. Consequences of
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
stereotyped and not decomposable into phases. atonic seizures frequently involve falls and injury.
There can be synchronous (or asynchronous) involve- Atonic seizures occur in both generalized and focal
ment of motor signs. They can be isolated events or epilepsies and are a cardinal semiology in Lennox
occur in a repetitive fashion. When they do occur, Gastaut syndrome. Their occurrence in focal
they do so at the same rate of contraction, and in the seizures suggest motor and premotor cortex involve-
various muscle groups in the body. The commonly ment [57].
used term tonic-clonic is an elementary sequence of
motor signs. 3.3.1. Negative myoclonus
Negative myoclonus is used to describe a brief
3.1. Akinetic interruption of muscle tone (<500 msec), like atonic
seizures. This results in a sudden brief lapse in
Akinetic motor signs are those characterized by the movement that may grossly appear like a “positive”
inability to perform voluntary movements with myoclonic jerk which is manifest as a single lighten-
preserved postural tone and awareness. It is a rare ing-like jerk (see 3.5). However, the pathogenesis is
ictal phenomenon and must be distinguished from different [58]. It can occur in a heterogeneous group
motor and behavioral arrest with staring, impaired of epilepsy syndromes disorders, ranging from self-
awareness, and motor arrest. Akinetic motor signs are limited syndromes, atypical self-limited childhood
without strong localizing or lateralizing value. Aki- epilepsy with centrotemporal spikes and electro-
netic motor signs are often associated with dystonic graphic status epilepticus in slow wave sleep, to focal
phenomena (see 3.8), but it can also evolve to include epilepsies involving lesions of the mesial frontal
progressive loss of muscle tone (see 3.3). Muscle tone structures (as in neuronal migration disorders), and
may be lost, but akinesia dominates the semiology. severe static or progressive myoclonic developmental
The same phenomenon can be observed for speech and epileptic encephalopathies.
production (aphemia or speech inhibition). Ictal
akinesia can manifest by an abrupt freezing of one’s 3.4. Eye blinking
gait initiation and may be precipitated by startle [52].
Akinetic motor signs and aphemia must be distin- Ictal eye blinking consists of a series of repetitive tonic
guished from ictal paresis and aphasia respectively contraction of the eyelids during a seizure. This
(see 3.11 and 7.2). Aphemia is characterized by the occurs without any other facial muscle contraction. Its
inability of articulation, including other movements of pathogenesis suggests activation of the trigeminal
the oro-laryngofacial muscles (i.e., inability to purse nerve fibers associated with the blink reflex [59]. Ictal
the lips, stick out the tongue open the mouth or eye blinking must be separated from repetitive facial
swallow voluntary in the presence of preserved clonic jerks that are observed during motor seizures,
comprehension). Akinetic signs are likely to occur as well as from eyelid myoclonia (often associated
during seizures that involve “negative motor” areas with a sustained upward gaze – see next sub-section).
(i.e., mesial premotor cortex and inferior frontal gyrus) The localizing significance of eye blinking remains
[53-55], and can be produced by direct electrical uncertain – though it seems over-represented in
stimulation of the same regions [55, 56]. patients with posterior quadrant epilepsies [60]. Its
lateralizing value, when unilateral, suggests an ipsilat-
3.2. Astatic eral epileptogenic hemisphere [61]. Unilateral ictal
eye blinking is believed to result from cortical blink
Astatic seizures (a.k.a. ”epileptic drop attack”) refer to inhibition of the contralateral eye, due to seizures in
a sudden loss of maintaining an erect posture. This the frontotemporal region [61].
3.5. Myoclonic / 3.6. Clonic leg. The dystonic posture can manifest as flexion or
extension and be proximal or distal, frequently with a
Myoclonic jerks (a.k.a. myoclonus) are a sudden, brief rotatory component. In the context of patients with
(<100-msec) involuntary, single or multiple contrac- temporal lobe epilepsy, unilateral ictal dystonia of the
tion(s) of muscle(s) or muscle groups of variable upper limb almost always lateralizes to the hemi-
topography. The term clonic (synonym rhythmic sphere contralateral to the seizure onset zone [68-70].
myoclonic) should be preferred to account for This sign, however, may have a weak interrater
myoclonic jerks that are regular and repetitive, at a reliability when temporal and extratemporal lobe
low frequency that is typically 0.2-5 Hz. They involve epilepsies are mixed [64] and may be related to ictal
the same muscle groups and vary in duration but are propagation and involvement of the basal ganglia
commonly prolonged. These elementary motor phe- following seizure onset [71].
nomena can occur both in generalized and in focal
seizures. In generalized seizures, they are usually 3.9. Gyratory
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
patients with temporal lobe epilepsy [81], and “symmetrical and sustained (>3-sec) lowering of labial
postictal Todd’s paresis (see 9.2). A proper diagnosis commissures with contraction of the chin, mimicking
therefore necessitates video-EEG to test the patient an expression of fear, disgust, or menace” [88]. This
[18] and confirm the ictal origin of the motor deficit. produces a facial expression that is recognized by a
Ictal paresis is almost always contralateral to the turned down mouth that appears as an inverted smile.
seizure onset zone and is likely to be produced by Seizures involving this semiology have been termed
seizures that occur in close vicinity to the primary chapeau de gendarme due to the shape of the hat
motor cortex [82]. used by French police (gendarme) during the reign of
Napoleon. When it occurs early during seizures, it has
3.12. Epileptic spasm a strong localizing value to the frontal lobe [89],
especially the anterior prefrontal and anterior cingu-
An epileptic spasm describes a seizure comprised of late cortices [88, 90]. However, other localizations
sudden flexion, extension, or mixed extension-flex- have also been described [91-93].
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
sequence of bilateral and symmetrical tonic posturing It is important to differentiate asymmetric clonic
with arms extended in supination, as in decerebrate ending from asymmetric amplitude of the jerks
posturing (suggesting involvement of the ictal dis- between the two sides of the body, as this alone
charge in the brainstem), followed by bilateral clonic should not be considered as asymmetric clonic
jerking with gradually decreasing frequency, which is ending.
generated by progressively longer silent periods
interrupting sustained tonic activity from inhibition 3.15. Versive
of muscle activation waning until the seizure stops
[97]. GTCS type 2 involves a tonic and clonic sequence Version must be used only to describe an unnatural,
that is often superimposed. When the two phases are forced and sustained movement of the eyes, head,
sequential, the clonic phase has a rhythmic quality trunk or whole body to one side. Small lateral saccadic
that is more sustained, without the exponential and clonic features can be superimposed during
dynamic changes observed in GTCS type 1 [97]. The version. During head-turning, the chin may move
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
motor features in GTCS type 2 suggest primary laterally but also upward or downward, depending on
involvement of the pre-motor and/or motor cortex, the muscles involved. Occasionally, seizures with
rather than propagation of the ictal discharge to the version can lead the patient to rotate around the long
subcortical and brainstem structures. This is further body axis. In this case, the term gyratory is applied
denoted by awareness that is partially retained in rare (see 3.9). Ictal version does not refer to a gaze
patients with GTCS type 2. Furthermore, the same preference or to other situations where the patient’s
clinical sequence described in patients with GTCS eyes, head or trunk deviate to one side (see 3.16). Ictal
type 2 can be observed unilaterally and asymmetrical- body turning is a term that encompasses different
ly typically pointing to a contralateral seizure onset semiological signs. Ictal version can be seen with focal
zone. Finally, a GTC type 2 can evolve into a GTCS seizures arising from any location. Their lateralizing
type 1, in which case the latter is described as the significance varies depending on the type of version
main semiology of the seizure. GTCS type 1 leads and whether it involves the eyes, head, or body, and
to postictal EEG suppression more frequently whether they are conjugate, sequential, and accom-
than GTCS type 2 [96]. This suggests that patients panying signs that occur [102]. Isolated version
with GTC type 1 might be associated with a higher risk involving the eyes likely involves the contralateral
of SUDEP. frontal eye fields. Direct electrocortical stimulation
has supported this localization by reproducing the
3.14.1. Figure-of-4 sign
same clinical signs [103]. However, when initial visual
The figure-of-4 sign may occur at the onset of the tonic
illusions / hallucinations are congruent with ocular
phase prior to the clonic phase in patients with FBTC
version, this suggests seizures arise from a contrala-
seizures. This semiology consists of unilateral tonic
teral occipital lobe origin. Head version strongly
extension of one arm and tonic flexion of the
lateralizes to the contralateral hemisphere when it is
contralateral arm. The latter may be held in front or
associated with neck extension and occurs in the first
behind the extended arm. This sign is considered to
10 seconds of a FBTC seizure [64, 104, 105]. In the
have a good lateralizing significance [64, 98] with the
situation where two successive head versions occur
extended arm occurring contralateral to the hemi-
prior to a FBTC seizure, it is the movement immedi-
sphere involved in seizure onset. The sequence of
ately preceding the tonic-clonic phase that prevails as
motor signs is important and can be complex, with
the lateralizing sign.
tonic extension of one limb first, followed by the
figure-of-4 sign pointing to the other hemisphere. In
this situation, it is the first manifestation of arm 3.16. Head orientation
extension that prevails to lateralize the seizure onset
zone. Non-versive turning of the head and eyes is a
frequent, but not specific sign when determining
3.14.2. Asymmetric clonic ending lateralization and localization. When it occurs early in
This sign refers to the terminal expression involving temporal lobe seizures, it is often ipsilateral to the
clonic jerks following a focal-to-bilateral-tonic sei- focus [106].
zure. When convulsive seizures terminate asymmet-
rically with unilateral clonic jerks that persist on one
side of the body, this has good lateralizing signifi- 4. Complex motor behaviors
cance for seizure onset. The last unilateral clonic
activity that persists occurs ipsilateral to the hemi- Complex motor behaviors refer to a heterogeneous
sphere of seizure onset, regardless of lobar localiza- group of motor signs and sequences. While some may
tion including temporal or frontal origin [64, 99-101]. look voluntary, the patient has no capacity to control
them during the seizure and they are inappropriate manipulating movements) can be self-directed (virtu-
for the situation. Gestures involving complex motor ally independent of environmental influence) or
behavior may or may not resemble natural move- involve more than self (environmentally influenced).
ments. They can be mixed with elementary In the context of temporal lobe epilepsy, unilateral
motor signs and may be associated with facial manual automatisms lateralize to the ipsilateral hemi-
expressions and verbalization or vocalization sphere mainly when associated with a contralateral
congruent with the motor pattern [107]. The patho- hand dystonia [111].
physiology of complex motor behaviors is unclear
4.1.3. Genital automatisms
and possibly depends on the type of motor involve-
Gestural automatisms are directed to involve the
ment. Features that occur during seizures with
genital region. These complex motor behaviors
complex motor behaviors could be due to a release
may appear with a sexual appearance including
phenomenon of stereotyped inborn networks
fondling, grabbing, scratching among other beha-
with fixed action patterns (central pattern genera-
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
the stimulation) and then bilateral [121, 122]. A movement. The overall resulting appearance of the
tendency for ictal laugh, though without overt motor behavior can be integrated with physiologic
laughter (hence not qualifying as a gelastic seizure), movement, though may be exaggerated during a
has been described in patients with small hypotha- motor sequence and be aligned with a facial expres-
lamic hamartomas [123]. sion and vocalization. It may also be non-integrated
Other mimic automatisms are rarely identified but appearing unnatural and separated from other
include the expression of negative (e.g., biting, fear, behavioral features [107]. Hyperkinetic behaviors
sadness) [124, 125] and positive (i.e., kissing) emo- are often produced by seizures arising from the
tional valences [126], or musical automatisms (e.g., frontal lobe [137-139]. In frontal lobe epilepsies, the
humming and whistling) [127-129]. behaviors exhibit a clinical continuum. Seizures with
hyperkinetic behavior may originate from the
4.1.7. Oroalimentary automatisms
rostral prefrontal regions, where highly integrated
Oro-alimentary automatisms including chewing, lip
behaviors predominate, or arise from the premotor
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
comprising the anterior superior temporal gyrus and lingula and ventral temporal cortex. Ictal visual loss is
the planum temporale without clear lateralizing value thought to reflect a disruption of function in the
[143, 146]. calcarine sulcus. This may be either unilateral or
bilateral. Regarding the visual loss, concentric
5.2. Visual symptoms changes of visual fields have a different localizing
value and would point towards a more anterior basal
Visual symptoms may be composed of either positive or medial temporal disturbance [151]. Illusions such as
or negative phenomena during seizures. Positive dyschromatopsia and blurring appears to be more
elementary phenomena are comprised of static or specific for the ventral and medial temporal structures
moving unformed flashes of lights, “spots”, or [148] and often reflects a right hemispheric lateraliza-
“blobs”. They may be white, black or include color, tion. Illusions of movement (kinetopsia) are repre-
remain localized or be non-localized within a visual sented by a disturbance of the lateral occipital and
field (i.e., quadrantic, hemi-field, or occupy the whole lateral occipito-temporal junction [153]. Illusions of
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
visual field) [147-149]. Negative elementary phenome- size (e.g. micropsia, macropsia and the Alice in
na correspond to transient amaurosis of the entire Wonderland syndrome), shape (metamorphopsia)
visual field or scotoma when it is confined to part or number (polyopia) suggest a disturbance in the
of it (quadrantanopia, hemianopia, tunnel vision) posterior medial parietal region (pre-cuneus and
[147, 148, 150, 151]. Intermediary visual hallucinations occipito-parietal sulcus). Elaborate hallucinations of
are more complex. They may appear as geometric faces point towards a disturbance of the right cuneus,
forms (i.e., stars, circles, triangles, squares, diamond) occipito-parietal sulcus, and the pre-cuneus and
[148, 150] and possess a slightly different sub-lobar fusiform gyrus [148]. Other elaborate hallucinations
localizing value [148]. Visual illusions comprise a great (places, persons, body parts, scenes) would reflect a
variety of visual phenomena affecting an object or its disturbance of the basal and medial temporal
visual background. This spans from visual blurring to structures [151, 157]. Prosopagnosia and distortion
an alteration of size (micropsia/macropsia), color of facial perception are the only reported elaborate
(dyschromatopsia), shape (metamorphopsia), dis- visual deficits described and point to the right
tance or movement (kinetopsia), and number (diplo- temporo-basal/fusiform and inferior occipital gyrus
pia, polyopia) [147, 148, 151-154]. Palinopsia refers to [155, 160, 161].
the persistence or recurrence of a visual object when
the stimulus is no longer present. Elaborate visual 5.3. Gustatory symptoms
phenomena refers to unimodal visual hallucinations
with detailed and meaningful implications such as Gustatory symptoms represent abnormal paroxysmal
faces, people, body parts, animals, and images of tastes within the mouth or in the throat. These are
scenes that occur without a clear mnemonic or usually unpleasant, and may be reported as salty,
affective component, as well as unimodal visual metallic, bitter, sour, acidic or indescribable [162, 163].
hallucinations associated with elaborate negative Gustatory symptoms are sometimes difficult for
phenomena which is dominated by the presence of patients to separate from olfactory symptoms and
prosopagnosia [148, 155-157]. may be associated together in the same subjective
Visual phenomena are a key feature of occipital experience during a seizure.
seizures occurring in 68 - 88% of patients [158, 159]. Gustatory symptoms during seizures are rare (occur-
However, they are not specific for occipital localiza- ring in around 4-8% cases) [162, 164]. They have been
tion and may occur less frequently during parietal, reported in seizures from peri-rolandic, insular and
anterior ventral and medial temporal and occipito- opercular regions, and less frequently from the medial
temporal lobe seizures. Elementary visual hallucina- temporal structures (amygdalohippocampal complex)
tions may reflect the transient disturbance in the without clear lateralizing value [144, 162, 165-167].
calcarine sulcus (primary visual cortex) caused by
seizures, but they may also arise from the lingula, 5.4. Olfactory symptoms
cuneus, and fusiform gyrus. Less often, they arise
more anteriorly from the lateral, basal and medial Olfactory symptoms are defined as a paroxysmal
temporal structures [148, 149]. When located in the unexplained sense of smell. These are usually, but not
center of the visual field, they reflect the disturbance always, unpleasant and can be neutral or even
of the calcarine sulcus. When elementary visual pleasant experiences. Olfactory hallucinations can
symptoms are unilateral, they occur contralateral to be described as an odor of burning, sulfur, alcohol,
the site of seizure onset. Intermediate hallucinations gas, garbage, barbecue, flowers, among other descrip-
have the same localizing and lateralizing value except tions, or be indescribable [168, 169]. These olfactory
that they reflect the disturbances of more anterior symptoms are sometimes difficult to differentiate
from gustatory symptoms by the patients and may be secondary somatosensory area in the parietal oper-
associated in the same subjective ictal experience. culum. Contralateral or bilateral sensory symptoms
Olfactory symptoms during seizures are rare, consti- have also been reported to originate in the supple-
tuting about 0.6% - 16% of all subjective manifesta- mentary sensorimotor area, the superior frontal gyrus
tions [168]. and cingulate motor area [176], and in the posterior-
Olfactory symptoms have been reported mostly in superior part of the insula [145].
seizures arising from medial temporal structures Painful somatosensory auras are described by patients
involving a range of etiologies including tumor and as acute and intense pain (burning sensation, pricking
hippocampal sclerosis though without lateralization ache, throbbing pain or muscle tearing sensation),
value [170, 171]. Electrical cortical stimulation studies affecting the body. Painful auras most often lateralizes
refined and extended these correlations and evoked the hemisphere involved at seizure onset [177].
olfactory symptoms in the medial temporal structures, Painful sensory auras may secondarily produce the
especially the amygdala, piriform cortex and uncus motor behavioral manifestations of pain, involving a
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
[172], near the olfactory bulb in the medial orbito- corresponding facial expression, verbal complaints
frontal cortex [169], mid-dorsal insula, and around the including shouting and crying, movements in an effort
insular central sulcus [163]. Olfactory auras have no to avoid a perceived stimulus, or autonomic changes
lateralizing value. such as facial pallor or flushing. Painful auras strongly
suggest involvement of the posterior insula and
5.5. Somatosensory symptoms parietal operculum [178]. Painful auras typically are
contralateral to seizure onset but they may be bilateral
Somatosensory symptoms may be described as or even ipsilateral when the painful sensation centers
tingling, numbness, electrical, shock-like sensation, in the face and trunk [179].
pain, or sense of movement [3]. They can be classified Segmental sensory auras involving temperature such
according to the localization and the quality of as warmth and cold are usually described as unpleas-
symptoms as unilateral paresthesia or numbness that ant. They often are unilateral when involving a limb,
follows a somatotopic pattern or displays a “Jackso- and seem to be associated with either somatosensory
nian march” in a segmental unilateral or bilateral or painful auras [180]. They are believed to point to the
distribution or as a painful somatosensory aura or same regions as those associated with painful auras.
sensation of heat [147, 166]. They should be differentiated from a non-localized
Somatosensory auras typically occur in patients with non-lateralized cold sensation associated with shiver-
parietal lobe seizures and represent the most ing which suggests localization in the amygdala.
frequently described aura arising from this region Ictal headache should be strictly differentiated from a
(in 29-63% cases) [165, 173, 174]. They are mostly painful somatosensory aura because they are thought
unilateral sensations, contralateral to the epilepto- to reflect a vascular mechanism rather than an
genic zone [4] but may also occasionally be bilateral or electrophysiologic disturbance involving a localized
even uni- and ipsilateral to seizure onset in 5% and cortical somatosensory area responsible for pain
2.5% of people, respectively [165]. [177]. It does not have localizing value [14] when it
Based on cortical electrical stimulation studies, is encountered, but is more likely to be ipsilateral to
unilateral paresthesia or numbness following a the seizure onset when it occurs in patients with
somatotopic pattern typically point towards the temporal lobe seizures [181].
contralateral primary somatosensory cortex on the
posterior bank of the central sulcus. Face and superior 5.6. Vestibular symptoms
limb paresthesia represent the most common locali-
zation (reflecting the large representation of these Vestibular symptoms may be defined as a sensation of
body parts in the sensory homunculus) and involve spinning or motion involving the body, with or
lateral neocortex, while lower limb paresthesia point without a sensation of unsteadiness [182]. This illusion
towards medial involvement [175]. If the involvement of motion might be described as rotatory symptoms in
of the paresthesia occupies one side of the body, then the up-down or left-right plane, a sense of movement,
seizures are most likely to arise contralateral to the floating, or undefinable sense of body motion [183]. In
involved upper and lower limbs. When involvement practice, it can be difficult to delineate the semiology
of the paresthesia is bilateral, seizures are more likely of vestibular symptoms and differentiate them from
to involve the midline body parts, especially the face the general non-specific term of dizziness that are
and trunk [175]. vague and ill-defined sensations. Vestibular auras are
Unilateral or bilateral paresthesia or numbness of rare, yet important symptoms reported with the
upper and lower limbs with segmental localization highest prevalence in patients with parietal lobe
without a sensory march typically point towards the seizures [165, 173]. However, they are not specific and
may also be encountered in patients with temporal symptomatology such as dreamy state (“mental
[144, 171], occipital [184], insular [167] and occasional- diplopia”), autoscopy, affective signs or symptoms,
ly frontal lobe seizures. At a sub-lobar level, focal or conscious automatic behavior. Therefore, it is not
cortical electrical stimulation studies during SEEG specific regarding localization and has been reported
emphasize the importance of the posterior perisylvian in frontal, temporal, insular, parietal and occipital lobe
region involving the supra-marginal gyrus, inferior seizures. Depersonalization needs to be differentiat-
parietal lobule, angular gyrus, superior and middle ed from derealization, which refers to the altered
temporal gyri, pre-cuneus, and insula. Vestibular perception of one’s surroundings that is experienced
phenomena have no consistent lateralizing value. as a sensation of unreality.
Somatagnosic auras result from a disturbance of Forced thinking is defined as involving intrusive
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
unimodal somatosensory (proprioceptive and tactile) thoughts, ideas, or words in people and should be
self-representation of the body. Autoscopic symp- differentiated from both a dreamy state and complex
toms result from a disturbance of multimodal self- sensory hallucinations [190, 191]. According to some
integration of body including visual perception of authors, the definition also includes an overwhelming
one’s body, either from an internal perspective of impulse to perform a certain act [192]. Due to the low
the body (autoscopic hallucination), or from an number of cases in the studies, the lateralizing and
external perspective (out-of-body-experience), or localizing value of ictal forced thinking remains
when patients cannot decide whether one’s self is uncertain. Most likely, the symptomatogenic zone
located inside the physical properties of the body or resides in the dominant frontal lobe [190].
reside outside of it (heautoscopic hallucination) [185].
Somatagnosic auras comprise non-visual, illusions of
the body such that one feels disconnected, dislocated 6. Affective (emotional) features
or a sense of movement, experiences phantom limbs
or reduplication, or deformity involving a body part Affective semiologies encompass an alteration in
[185]. These are rare but suggest a non-dominant mood or an apparent emotional experience or
(right) temporo-parietal junction as the site of seizure observation that is manifest by patients during
involvement [186]. seizures. Often, these subjective ictal symptoms are
Autoscopic hallucinations are rare, tend to be more reported at the onset of the seizures and may be
often perceived in the contralateral visual field and followed by other semiologies. When motor signs
suggest right (non-dominant) medial occipitoparietal occur simultaneously with them, the expression of an
cortex (pre-cuneus and occipito-parietal sulcus) affective (emotional) feature is classified under mimic
involvement [148, 187]. automatisms (see 4.1.6). The majority of ictal experi-
An out-of-body-experience typically points to the ences of emotion are unpleasant, such as anxiety and
non-dominant lateral parietal lobe [174, 186], but also fear (60%), and depression (20%), while ictal joy is only
may occur with seizures arising from the dominant rarely reported [193]. In one study, across all regions
temporoparietal region [188]. of interest, 58% of reported subjective affective
experiences were negatively valenced and unplea-
5.8. Depersonalization sant, whereas 15% of experiences were positive and
pleasant [194]. Clinical observations have often
Depersonalization is defined as the detachment from reported that patients with seizures arising from
oneself, either the mind or body. In addition, this may limbic structures lateralized to the right side of the
involve being a detached external observer of oneself brain have a higher incidence of emotional distur-
during a seizure. Depersonalization is not at all bances, such as fear and anxiety, than those who have
specific to epileptic seizures. It is classified as a seizures arising from the left side [195]. The emotions
symptom according to the DSM-5, involved in a with negative valence are most often formed from the
dissociative disorder [189], and is often encountered left (dominant) hemisphere, and those with a positive
in anxiety and panic disorders, as well as obsessive- or pleasant valence (or neutral valence) [196] are most
compulsive disorder, severe stress, use of recreational often lateralized to the right (non-dominant) hemi-
drugs and even in normal people following severe sphere [193, 196]. In 100 children, based on a study to
sleep deprivation. There is a phenomenological assess the value of focal seizures, emotions with
overlap between autoscopic phenomena (out-of- positive (pleasant) character were significantly more
body experience) and depersonalization. When asso- frequent during right-sided seizures while negative
ciated with epilepsy, it is associated with various ictal emotions did not lateralize the seizure onset zone.
Emotional semiologies are typically associated with seizures lateralized to limbic structures on the left
involvement of the limbic structures. The best-known side [195]. However, there have been some inconsis-
examples of affective symptoms are fear and anxiety. tent reports regarding the lateralizing value of ictal
These are generally considered to reflect involvement anxiety [203-207] making lateralization less distinct.
of the amygdala during temporal lobe seizures. Video- Seizures with anxiety when they arise from the mesial
EEG monitoring identified affective auras in 18% of 184 temporal structures involve the limbic network and
patients with temporal lobe epilepsy who underwent especially the amygdala, [172, 204, 208-210]. However,
resective surgery [197]. In this study, affective aura was they may also be widely distributed within the
unable to lateralize or localize the seizures. They were temporal lobe [211], including the temporal neocortex
more likely to be negative auras (15%) than positive and any of the limbic structures (i.e., amygdala,
(3%) while ictal affective behavior was present in 22% hippocampus and parahippocampal gyrus) [212].
of patients (10% positive, 14% negative) [197]. Overall, the best examples of ictal anxiety are
generally considered to reflect involvement of the
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
lation). They can also occur in seizures arising from [241] as well as the hypothalamus [242] in a case report
the mesial temporal region [120], orbito-frontal cortex have been reported, though in the latter case, this was
[196], and the anterior insula in a single patient during felt to be likely due to activation of the insula. Most
electrical stimulation studies [228]. Seizures associa- have been described with focal epilepsies, but a case
ted with sadness often accompany seizures with was reported with generalized epilepsy induced by
laughing in the setting of a hypothalamic hamartoma. watching television [243].
Focal seizures associated with sadness may be
accompanied by lacrimation, sad facial expressions 6.7. Mystic
and sobbing when they arise from a hypothalamic
hamartoma [229]. Mystic seizures or experiences with altered state of
consciousness impart a religious or spiritual meaning
6.5. Guilt to a person during seizures. This experiential affect
involves a sensation that the person becomes one
Guilt is an affective symptom involving an emotional with God or believes in the spiritual apprehension of
feeling of having done wrong or failed in an truth that is beyond the intellect. Religious attribu-
obligation. No clear data is available regarding tions are rarely divulged though may include clair-
possible lateralizing value and therefore the laterali- voyance, telepathy, autoscopy, religious phrases,
zation is uncertain [213], though considering the prayer, being in the presence of God, and auditory
valence, it possibly points to the left hemisphere or visual hallucinations of religious figures [232].
[196, 230]. Given the paucity of information regarding There is a predominance of right lateralization as the
guilt and focal seizures, there is insufficient localizing critical site of religious experience due to the
information. emotional nature [244]. Mystical experiences have
been most often linked to the temporal lobe
6.6. Ecstatic feeling / bliss [234, 245, 246]. Mystic, religious, and spiritual experi-
ences have also been reported to involve neocortical
Focal aware seizures with a positive affective compo- areas when visual and auditory hallucinations or
nent are infrequently characterized by ecstasy or a complex ideation occur [246].
sense of bliss, and more commonly involve negative
sensations such as fear, anxiety, or panic. Ecstatic 6.8. Sexual
seizures evoke a feeling of bliss and intense positive
emotion, enhanced physical well-being, and clarity Sexual experiences of desire, arousal or orgasmic aura
with heightened self-awareness or perception of the may infrequently be involved in the ictal features of
external world with an overwhelming feeling or focal epilepsies. They are more often observed in
expression of happiness or joyful excitement. An women [247]. Sexual auras do not have strong
ecstatic phenomenon is an altered state of conscious- lateralizing value though most arise from the right
ness with a sense of “hyper-reality”, and complete hemisphere [248]. Sexual auras often stem from the
present-moment awareness with a feeling of union mesial temporal structures [248, 249] but also have
with the universe [231]. Pleasure has been described been noted arising from the anterior cingulate cortex
as elation, intense pleasure, serenity, gladness, joy, [194]. For seizures marked by sexual automatisms such
exhilaration, and completeness [227]. Left lateraliza- as masturbatory behavior, pelvic thrusting or similar
tion was suspected and an overlap with right automatisms, although typically attributed to tempo-
lateralization with the presence of religious overtones ral lobe disease, frontal lobe seizures using depth EEG
[232], though consistent lateralization has not been electrodes have also been described [250].
Ascertaining this semiology feature is important, as it different patterns of ictal aphasia were identified:
allows determining awareness of the patient during impaired comprehension was associated with poste-
seizures. This helps classify focal seizures based on the rior lateral involvement, anomia and reduced verbal
current ILAE seizure classification system [5]. In fluency with the anterior mediobasal structures,
practical terms, if a patient cannot recall events during whereas Wernicke’s aphasia with rapid verbal output
a focal seizure, then the seizure is classified as a focal (“jargonaphasia”) was found with basal temporal
impaired awareness seizure. However, ictal amnesia involvement [253]. However, in a large study involving
and awareness are not completely synonymous, ictal aphasia in patients with focal epilepsies, this
because, exceptionally, seizures can present with semiological presentation had limited localizing value
isolated ictal amnesia, yet with clear awareness [251]. within the dominant hemisphere and was most
However, detailed observation is required to distin- commonly seen in patients with seizures originating
guish and separate these two cognitive semiologies [5]. from the parieto-occipital regions, and even with
7.1.2. Déjà / jamais vu / dreamy state seizures spreading from the non-dominant to domi-
These experiential phenomena consist of: (1) déjà vu or nant language areas of the brain [254].
a feeling that one has lived through the present
situation before; (2) jamais vu as the feeling one has 8. Autonomic seizure semiology
experienced the situation for the first time, despite
having been in the situation before; (3) a dreamy state Autonomic symptoms and signs are common accom-
with vivid memory-like hallucinations. These symp- panying features of focal or generalized seizures, and
toms suggest a symptomatogenic zone in the temporal these include cardiovascular (palpitations, tachycar-
lobe, primarily the mesial structures (amygdala and dia), respiratory (hyperventilation), cutaneous (feel-
hippocampus) and the sub-hippocampal structures ings of heat of cold, piloerection), gastrointestinal
(rhinal cortices), without lateralizing value. The tempo- (bloating or nausea, retching and vomiting) and
ral neocortex might also play a significant role in genitourinary (urinary urge, sexual arousal) phenom-
producing these phenomena. Of note, these symptoms ena. When autonomic signs occur early and promi-
are not specific to patients with epilepsy and can occur nently in a focal seizure, then the event is recognized
in other neurologic and psychiatric conditions [172]. as a focal autonomic seizure (a subset of focal aware
7.1.3 Derealization seizures- non-motor) [5]. Some autonomic phenome-
Derealization refers to the altered perception of one’s na, such as ictal vomiting, ictal urinary urge or
surroundings that are experienced as unreal. It should coughing, may have lateralizing or localizing value.
be differentiated from depersonalization (see section When ictal symptoms and signs are confined to the
5.8). Although usually reported in patients with autonomic nervous system, these may be mistaken for
psychiatric conditions (depression, anxiety), case non-epileptic events. It is also important to distinguish
reports and small case series have revealed derealiza- between subjective symptoms (autonomic auras) and
tion in epileptic seizures. Due to the low number of objective autonomic phenomena (autonomic seizure)
cases, the localization is uncertain, but it is most likely during seizures.
associated with temporal lobe epilepsy [252].
8.1. Cardiovascular manifestations
7.2. Aphasia
Common cardiovascular manifestations include
Ictal aphasia is the inability to comprehend or alterations in heart rate and rhythm, blood pressure,
formulate language during focal seizures. It is ECG changes and chest pain.
8.2.4. Piloerection
8.1.2. Bradycardia and ictal asystole Piloerection is defined as erection of the hairs of the
Bradycardia and ictal asystole are much less frequent skin due to contraction of the tiny arrectores pilorum
(0-2%) than ictal tachycardia [259-263]. This is usually muscles that elevates the hair follicles above the rest
observed in patients with temporal lobe seizures [264- of the skin, moving the hair vertically and appearing to
271], but also rarely arises from other areas, such as “stand on end” (gooseflesh or goosebumps). Piloer-
the left cingulate [272]. While some authors suggest ection is a rare sign that is seen in 0.40-0.65% of
left lateralization [265, 273], the majority of studies did patients in large VEM series [289, 290]. Piloerection is
not confirm a lateralizing value for ictal bradycardia usually associated with other autonomic symptoms,
[267, 268, 270, 271]. Bradycardia may occur in the such as sweating, flushing, and shivering. There is a
context of respiratory depression [274]. Falls and strong association with temporal lobe epilepsies
myoclonus were observed with prolonged ictal including the insula and amygdala. However, laterali-
asystole (mean: 14.8 7 s) [269, 275]. Thus, loss of zation is inconsistent [290-293]. Recent reports reveal a
muscle tone or bilateral asymmetric jerky limb strong representation of autoimmune encephalitis
movements during a seizure suggest the possibility and gliomas as a cause of seizures associated with
of ictal asystole [275]. piloerection [289, 293, 294].
without clear lateralizing significance [296, 303, 304]. frequently seen in epileptic seizures than in patients
Invasive EEG recordings in isolated cases have with non-epileptic events [258].
implicated the perisylvian frontal operculum [305]
8.4.1. Hypoventilation
and the insula [306].
Hypoventilation and oxygen desaturation of <90%,
8.3.3. Spitting <80% and <70% was observed in 33.2%, 10.2% and
Spitting is an infrequent symptom reported in 0.3-2% of 3.6% of all seizures recorded in patients with drug-
patients with temporal lobe seizures [296, 307-310], and resistant epilepsy, respectively [332]. Another study
several studies implicate non-dominant lateralization reported the presence of ictal hypoxemia in 70.8% of
[296, 310-312]. However, the left temporal lobe has also patients experiencing 79 seizures. In this cohort,
been involved in case reports [309, 313, 314]. In a case desaturation was mild (mean: 92.5%) in 46% of all
report evaluated with invasive EEG electrodes, although seizures, moderate in 39% (mean: 81.5%), and severe
the seizure onset zone was in the left mesial temporal in 14% (mean: 64.7%) [333]. Oxygen desaturation
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
lobe, the ictal spitting coincided with the propagation of lasting longer than 70 seconds with a nadir of 83% has
the ictal discharge to the right temporal lobe, implicat- been reported during focal seizures without evolu-
ing the latter as the symptomatogenic zone [312]. Direct tion to bilateral tonic-clonic seizures. This supports
electrical stimulation studies during invasive EEG the hypothesis of centrally mediated hypoventilation
monitoring have identified the entorhinal cortex as a during focal epileptic seizures [258].
site involved in ictal spitting [311]. Ictal spitting does not
8.4.2. Apnea
occur in association with ictal vomiting, ictal coughing,
Apnea was reported to occur in approximately 40% of
or ictal fear, suggesting there are different sites in the
seizures recorded in adult series with duration lasting
brain that mediate these symptoms with unique
for more than 10 seconds (range: 10-63 seconds; mean:
specificity [308]. Although ictal spitting has been
24 seconds) based on polygraphic measurements
reported as a gastrointestinal autonomic phenomenon,
[274, 333]. Prolonged central apnea (60 seconds)
it has a clear motor component and could also be listed
occurred in 6.3% of patients in association with severe
under automatisms.
hypoxemia during seizures with blood oxygen satu-
8.3.4. Vomiting ration levels (SpO2) of less than 75%. Similarly,
Vomiting is a striking feature when it occurs and is not episodes with ictal apnea have been reported in
uncommon in self-limited childhood occipital epilep- neonates and children with TLE [279, 334]. Central
sies. In adult patients evaluated for epilepsy surgery, apnea may precede seizure onset recorded on scalp
ictal vomiting has been reported in patients with TLE, EEG in more than a half of cases, and rarely persists
especially involving the mesial structures. Seizures into the postictal period. Patients typically do not
commonly originate from the right hemisphere [315- recall ictal apneas, and therefore this might remain
320], but also may involve the left temporal lobe [321- unrecognized without respiratory monitoring [333].
323]. A recent series on ictal vomiting failed to Oxygen desaturation less than 90% significantly
demonstrate consistent lateralization [324]. Intracranial correlated with temporal lobe localization at seizure
recordings have also suggested that the symptomato- onset, right hemispheric seizure lateralization, and
genic zone may reside in the anterior insula when contralateral hemispheric propagation [332]. The
vomiting results from propagation of the ictal activity degree of desaturation correlated with seizure dura-
from the mesial temporal structures to the insula tion and propagation and involved the contralateral
[325, 326]. hemisphere [335]. No significant differences were
seen between mesial and neocortical temporal lobe
8.3.5. Flatulence
seizure onsets [336]. On intracranial EEG recordings in
Flatulence is a rare symptom that occurs in 0.6% of
patients with mesial TLE, 68.4% showed ictal apnea,
patients [327]. It suggests temporal and insular
either accompanied by, or following seizure onset.
involvement during seizure propagation, but is
Apnea may be the principal or sole manifestation in
without any lateralizing value [327, 328]. According
15% of TLE cases [337].
to anecdotal reports, rare related gastrointestinal
symptoms including an ictal urge to defecate 8.4.3. Choking
[329, 330] and ictal burping [331] may localize to the Choking due to acute laryngospasm as an isolated
right temporal lobe. event associated with nocturnal seizures may rarely
represent an ictal manifestation [338]. Nocturnal
8.4. Respiratory dysfunction choking can occur in sleep-related hypermotor
seizures associated with nocturnal frontal lobe
Respiratory dysfunction, specifically hypoventilation epilepsy, and may be misdiagnosed as sleep apnea
(bradypnea), apnea, and oxygen desaturation, is more syndrome due to abnormal nocturnal motor activity
and excessive daytime somnolence [339]. Localizing 8.6. Urinary and genital ictal phenomena
information about ictal choking is sparse, however,
anecdotally, ictal choking observed during stimula- 8.6.1. Urinary sensations
tion studies has implicated the frontal operculum Urinary sensations are rarely an autonomic symptom
[340] and anterior insula [341, 342]. In patients with associated with focal seizures in which the patient
insular seizures, the semiology typically begins in develops an intense desire to urinate. The frequency
patients who are fully consciousness and experience a is estimated to range from 0.8 to 8% of patients
sensation of laryngeal constriction that is often [358]. It has been reported to arise from the non-
associated with unpleasant paresthesia, affecting dominant hemisphere and more specifically from the
large cutaneous territories [343]. temporal lobe [358-360]. There are some reports of
ictal single-photon emission computed tomography
8.4.4. Hyperventilation
studies that demonstrate hyperperfusion involving
Hyperventilation may occur during focal seizures.
the right temporal lobe (superior temporal gyrus) and
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
8.5.1. Miosis
Miosis is a rare autonomic sign that has been
9. Postictal phenomenology
described as a part of generalized photosensitive
Postictal neurological deficits and/or psychiatric signs
epilepsies [350] and in patients with focal epilepsies
and symptoms are often accompanied by diffuse or
involving the temporal, parietal and occipital lobe.
focal slowing or postictal generalized EEG suppres-
The localizing and lateralizing value for miosis in
sion after the clinical signs of the seizure have ended
patients with epilepsy is uncertain [351-354].
[364]. Many of these signs and symptoms are
8.5.2. Mydriasis attributed to intrinsic inhibitory mechanisms which
Mydriasis is a common sign seen bilaterally when it is contribute to seizure termination. The duration of a
associated with seizures in patients with either GTCS postictal state is variable and can be up to several days.
or FBTC seizures. This is due to widespread activation However, while some symptoms (headache, muscle
of the cortical and subcortical structures of the brain aches, postictal psychiatric symptoms) may last
that influence the sympathetic nervous system longer, most postictal features last 5-30 minutes
[295, 349]. Unilateral mydriasis is rarely reported to [365]. Prolonged postictal altered consciousness or
occur in patients with temporal lobe seizures prolonged postictal focal neurological deficits should
[256, 355] or occipito-temporal seizures, and appears raise the suspicion of ongoing seizures and non-
ipsilateral to the seizure onset zone [356]. It has also convulsive status epilepticus. In these cases, patients
been reported to occur in the contralateral pupil of a should be expeditiously evaluated with EEG [9, 11].
young boy with left frontal seizures [357]. Rarely, in the peri-ictal and postictal state, patients
may succumb to sudden unexpected death in sentence) occurred in 100% of 62 seizures, and
epilepsy (SUDEP) [366]. patients took more than 68 seconds to read a test
phrase correctly [380]. Overall, postictal speech
9.1. Unresponsiveness disturbances correctly lateralized to the dominant
hemisphere in 81.3% of all patients, regardless of
Unresponsiveness was the most common phenome- which kind of dysfunction was documented (i.e. no
non (mean frequency of 96%) in a recently published statistically significant difference, although one must
systematic review and meta-analysis of 45 studies on recognize the small groups of paraphasias).
the postictal state [367]. Recovery from postictal
unresponsiveness may take seconds to minutes [368]. 9.5. Nose wiping
Paresis (Todd’s paresis) may occur after focal motor or temporal lobe epilepsy [381-384]. It was shown to be
FBTC seizures. A large study showed postictal paresis in ipsilateral to the hemisphere of seizure onset in 86.5%
6% of FBTC seizures [369]. However, this could be an of patients with TLE, and patients with extratemporal
underestimate, due to often insufficient postictal lobe epilepsy performed ipsilateral nose wiping in
testing of the patients. Postictal paresis may last from 54.5% of all seizures [370].
minutes to hours [369]. It lateralizes to the contralateral
hemisphere, regardless of whether the seizure spreads 9.6. Headache
to the contralateral hemisphere on surface EEG or not
[370-373]. However, postictal paresis can also be Headache occurs in 41.6-66% of patients with seizures
bilateral. Postictal paresis develops after ictal involve- with a duration lasting from minutes to hours [367, 385].
ment of the motor cortex, most often in frontal lobe Younger age at seizure onset and longer duration of
seizures. However, it has also been documented in epilepsy, drug-resistant epilepsies, and tonic-clonic
seizures originating in temporal, parietal and occipital seizures are additional risk factors [386]. Postictal
lobes [374]. Sensory deficits following seizures have headache often manifests with severe migraine-like
been rarely reported and can be missed if sensation is features. In temporal lobe epilepsy, postictal headache
not specifically tested or symptoms addressed [375]. was found to be ipsilateral to the site of seizure onset in
90% of cases [387]. However, no significant lateraliza-
9.3. Blindness. tion value was found in patients with frontal lobe
epilepsies [388]. Peri-ictal headache was more likely to
Following seizures, loss of vision may occur on one be ipsilateral to the seizure onset in patients with
side of the visual field (hemianopsia) or both sides temporal lobe epilepsies (90%) than in those with
(amaurosis) [376, 377]. The duration typically lasts extratemporal lobe epilepsies (12%) [181].
from seconds to hours [367]. It has been reported in
two-thirds of patients with childhood occipital epi- 9.7. Palinacousis
lepsy of Gastaut [378]. Postictal blindness points to
involvement of the visual cortex and has been Palinacousis involving preservation of an external
described in patients with occipital and temporal auditory stimulus or retained fragment of a previously
lobe seizures. Ictal homonymous hemianopsia later- heard sentence may occur after seizure cessation.
alizes to the contralateral hemisphere [379]. These auditory illusions have been described in a few
cases, though the localizing and lateralizing value of
9.4. Language dysfunction this symptom is uncertain [389].
9.9. Psychiatric symptoms and syndromes Axial (trunk, including neck), proximal limb, distal
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
limb.
These include delirium, psychosis, catatonia, impaired
cognition and amnesia [368]. These do not have 10.4. Incidence
localizing or lateralizing value. Delirium, changes in
perception (hallucinations), thoughts (incoherence, The number of seizures within a time period or the
delusions) and catatonia may last for hours to days number of seizure days per unit of time (i.e., 3-4
[368, 393]. Postictal delirium may transition into seizures/month).
postictal psychosis, including violent bizarre or
sexually inappropriate behavior. The prevalence of 10.5. Cluster
postictal psychosis ranges between 2% and 7%,
independent of type of epilepsy [368, 394]. It can The incidence of seizures within a given period
develop after a “lucid phase” when the patient (usually one or a few days) that exceeds the average
recovers from initial postictal confusion, only to incidence over a longer period for the patient (i.e., 3-5
reappear six hours to a week later [395]. The mean seizures over 8 hours). Note that this definition does
duration of postictal psychosis is variable, lasting up to not apply to the presence of a cluster of epileptic
9-10 days (range: 12 hours - 3 months) without spasms (which denotes repetitive occurrence / series
treatment. Approximately a half of patients with of epileptic spasms).
postictal psychotic symptoms also have a history of
psychiatric disorders, such as depression, anxiety and 10.6. Provocative factor
attention deficit disorder [396]. Postictal psychosis
occurs more often after a cluster of GTCS [395]. Endogenous or exogenous elements that are capable
Postictal psychosis is a treatable condition, which left of triggering seizures in people with chronic epilepsy
untreated, is associated with serious patient-related and evoking seizures in susceptible individuals
morbidity and mortality [395]. Homicide during the without epilepsy. It is important to distinguish
postictal psychosis has been described in a single case facilitating factors that temporarily increase seizure
report [397]. Postictal depressive and anxiety symp- risk from precipitating factors (i.e., the specific
toms may occur for more than 24 hours and within triggers in reflex epilepsies). Acute symptomatic
five days following a seizure [398]. For focal epilepsy, seizures are often referred to as “provoked” seizures.
18% of patients showed postictal depressive symp-
toms, characterized by anhedonia, helplessness, self- 10.7. Prodrome
deprecation or suicidal thoughts. Postictal dysphoric
symptoms are more likely in temporal plus epilepsies, The subjective constellation of a non-specific, broad
compared to pure temporal lobe epilepsies [399]. spectrum of “warning” symptoms (such as an ill-
Postictal anxiety lasts from minutes to hours, and is localized sensation or agitation) that heralds the onset
often accompanied by depression. of an epileptic seizure but does not form part of it [3].
The duration is over 30-60 minutes, and it may persist
for up to several days prior to seizure onset.
10. Somatotopic modifiers and time-related
features
11. Conclusion
Some ictal phenomena can occur in different parts of
the body, hence the somatotopic modifiers should be Scalp and invasive video-EEG monitoring has been
added to the respective ictal phenomena [3, 5]. instrumental to update and define terminology, and
provide lateralizing and localizing significance to lateralization value is higher when more features are
semiology in patients with epilepsy. Often, several present. Ictal fear followed by hyperkinetic behavior
semiological features occur during the same seizure suggests seizure involvement of the frontal lobe,
(either simultaneously or in a sequence), due to while fear followed by distal gestural and oro-
propagation of the seizure within the network alimentary automatisms suggests a focus in the
(table 2). Seizure semiology is dynamically produced temporal lobe. Seizures starting in the posterior
by interconnected structures, in which specific quadrant of the brain (occipital and parietal lobes)
electrophysiologic interconnections, rather than often show rapid propagation to anterior structures
anatomical location, likely play an important role (frontal and temporal lobes) and may manifest
in clinical expression [400]. Seizure propagation without a visual aura. A detailed interview about the
within an epileptic network and the corresponding symptoms and possible occurrence of auras (includ-
evolution in time of the seizure semiology have ing those that occurred in the past but do not exist
been compared to “words in a meaningful sentence” anymore) may be important for determining localiza-
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
the ILAE Commission for Classification and Terminology. do absence, generalized, and nonmotor mean? Epilepsia
Epilepsia 2017; 58(4): 522-30. 2018; 59(3): 523-9.
6. Scheffer IE, Berkovic S, Capovilla G, Conolly MB, French J, 21. Guo JN, Kim R, Chen Y, Negishi M, Jhun S, Weiss S, et al.
Guilhoto L, et al. ILAE classification of the epilepsies: Impaired consciousness in patients with absence seizures
position paper of the ILAE Commission for Classification investigated by functional MRI, EEG and behavioural
and Terminology. Epilepsia 2017; 58: 512-21. measures: a cross-sectional study. Lancet Neurol 2016; 15
(13): 1336-45.
7. Lüders H, Acharya J, Baumgartner C, Benbadis S, Bleasel
A, Burgess R, et al. Semiological seizure classification. 22. Blumenfeld H. Consciousness and epilepsy: why are
Epilepsia 1998; 39(9): 1006-13. patients with absence seizures absent? Progr Brain Res 2005;
150: 271-603.
8. Blümcke I, Arzimanoglou A, Beniczky S, Wiebe S.
Roadmap for a competency-based educational curriculum 23. McPherson A, Rojas L, Bauerschmidt A, Ezeani CC, Yang
in epileptology: report of the Epilepsy Education Task Force L, Motelow JE, et al. Testing for minimal consciousness in
of the International League Against Epilepsy. Epileptic complex partial and generalized tonic-clonic seizures.
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
36. Jung R. Correlation of bioelectrical and autonomic 51. Langston ME, Tatum WO 4th. Focal seizures without
phenomena with alterations of consciousness and arousal awareness. Epilepsy Res 2015; 109: 163-8.
in man. Springfield, Illinois: Thomas, 1954.
52. Toledano R, García-Morales I, Kurtis MM, Pérez-Sem-
37. Kooi KA, Hovey HB. Alterations in mental function and pere A, Ciordia R, Gil-Nagel A. Bilateral akinetic seizures: a
paroxysmal cerebral activity. AMA Arch Neurol Psychiatry clinical and electroencephalographic description. Epilepsia
1957; 78(3): 264-71. 2010; 51(10): 2108-15.
38. Boudin G, Barbizet J, Masson S. Étude de la dissolution 53. Meletti S, Rubboli G, Testoni S, Michelucci R, Cantalupo
de la conscience dans 3 cas de petit mal avec crises G, Stanzani-Maserati M, et al. Early ictal speech and motor
prolongees. Rev Neurol 1958; 99: 483-7. inhibition in fronto-mesial epileptic seizures: a polygraphic
study in one patient. Clin Neurophysiol 2003; 114(1):
39. Tizard B, Margerison J. Psychological functions during 56-62.
wave-spike discharges. Brit J Soc Clin Psychol 1963; 3: 6-15.
54. Noachtar S, Lüders HO. Focal akinetic seizures as
40. Mirsky AF, Vanburen JM. On the nature of the “absence” documented by electroencephalography and video record-
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
in centrencephalic epilepsy: a study of some behavioral ings. Neurology 1999; 53(2): 427-9.
electroencephalographic and autonomic factors. Electro-
encephalogr Clin Neurophysiol 1965; 18: 334-48. 55. Lüders H, Dinner DS, Morris H, Wyllie E, Comair YG.
Cortical electrical stimulation in humans. The negative
41. Panayiotopoulos CP, Obeid T, Waheed G. Differentia- motor areas. Adv Neurol 1995; 67: 115-29.
tion of typical absence seizures in epileptic syndromes. A
video EEG study of 224 seizures in 20 patients. Brain 1989; 112 56. Lim SH, Dinner DS, Pillay PK, Lüders H, Morris HH, Klem
(Pt 4): 1039-56. G, et al. Functional anatomy of the human supplementary
sensorimotor area: results of extraoperative electrical
42. Inoue Y, Mihara T. Awareness and responsiveness stimulation. Electroencephalogr Clin Neurophysiol 1994; 91
during partial seizures. Epilepsia 1998; 39(S5): 7-10. (3): 179-93.
43. Lux S, Kurthen M, Helmstaedter C, Hartje W, Reuber M, 57. Scholly J, Bartolomei F, Valenti-Hirsch MP, Boulay C,
Elger C. The localizing value of ictal consciousness and its De Saint Martin A, Timofeev A, et al. Atonic seizures in
constituent functions: a video-EEG study in patients with children with surgically remediable epilepsy: a motor
focal epilepsy. Brain 2002; 125(12): 2691-8. system seizure phenotype? Epileptic Disord 2017; 19(3):
44. Cohen E, Antwi P, Banz BC, Vincent P, Saha R, Arencibia 315-26.
CA, et al. Realistic driving simulation during generalized
epileptiform discharges to identify electroencephalographic 58. Tassinari CA, Rubboli G, Parmeggiani L, Valzania F,
features related to motor vehicle safety: feasibility and pilot Plasmati R, Riguzzi P, et al. Epileptic negative myoclonus. Adv
study. Epilepsia 2020; 61(1): 19-28. Neurol 1995; 67: 181-97.
45. Naik PA, Fleming ME, Bhatia P, Harden CL. Do drivers 59. Saporito MAN, Vitaliti G, Pavone P, Di Stefano G, Striano
with epilepsy have higher rates of motor vehicle accidents P, Caraballo RH, et al. Ictal blinking, an under-recognized
than those without epilepsy? Epilepsy Behav 2015; 47: phenomenon: our experience and literature review. Neu-
111-4. ropsychiatr Dis Treat 2017; 13: 1435.
46. Nirkko AC, Bernasconi C, von Allmen A, Liechti C, Mathis 60. Lagarde S, Dirani M, Trébuchon A, Lepine A, Villeneuve
J, Krestel H. Virtual car accidents of epilepsy patients, N, Scavarda D, et al. Ictal blinking in focal seizures: Insights
interictal epileptic activity and medication. Epilepsia 2016; 57 from SEEG recordings. Seizure 2020; 81: 21-8.
(5): 832-40.
61. Kalss G, Leitinger M, Dobesberger J, Granbichler CA,
47. Giacino JT, Kalmar K, Whyte J. The JFK coma recovery Kuchukhidze G, Trinka E. Ictal unilateral eye blinking
scale-revised: measurement characteristics and diagnostic and contralateral blink inhibition – a video-EEG study and
utility. J Phys Med Rehabil 2004; 85(12): 2020-9. review of the literature. Epilepsy Behav Case Rep 2013; 1:
48. Giacino JT, Katz DI, Schiff ND, Whyte J, Ashman EJ, 161-5.
Ashwal S, et al. Practice guideline update recommendations 62. Bonelli SB, Lurger S, Zimprich F, Stogmann E, Assem-
summary: disorders of consciousness: report of the Guide- Hilger E, Baumgartner C. Clinical seizure lateralization in
line Development, Dissemination, and Implementation frontal lobe epilepsy. Epilepsia 2007; 48(3): 517-23.
Subcommittee of the American Academy of Neurology;
the American Congress of Rehabilitation Medicine; and the 63. Janszky J, Fogarasi A, Jokeit H, Ebner A. Lateralizing
National Institute on Disability, Independent Living, and value of unilateral motor and somatosensory manifesta-
Rehabilitation Research. J Phys Med Rehabil 2018; 99(9): tions in frontal lobe seizures. Epilepsy Res 2001; 43(2):
1699-709. 125-33.
49. Laureys S, Gosseries O, Tononi G. The neurology of 64. Marashly A, Ewida A, Agarwal R, Younes K, Lüders HO.
consciousness: cognitive neuroscience and neuropathology. Ictal motor sequences: lateralization and localization values.
Academic Press, 2015. Epilepsia 2016; 57(3): 369-75.
50. Cavanna AE, Monaco F. Brain mechanisms of altered 65. Jeavons PM. Nosological problems of myoclonic epilep-
conscious states during epileptic seizures. Nat Rev Neurol sies in childhood and adolescence. Dev Med Child Neurol
2009; 5(5): 267-76. 1977; 19(1): 3-8.
66. Vaudano AE, Ruggieri A, Tondelli M, Avanzini P, Benuzzi 84. Loddenkemper T, Kotagal P. Lateralizing signs
F, Gessaroli G, et al. The visual system in eyelid myoclonia during seizures in focal epilepsy. Epilepsy Behav 2005; 7
with absences. Ann Neurol 2014; 76(3): 412-27. (1): 1-17.
67. Doose H. Myoclonic-astatic epilepsy. Epilepsy Res Suppl 85. Job AS, De Palma L, Principe A, Hoffmann D, Minotti L,
1992; 6: 163-8. Chabardès S, et al. The pivotal role of the supplementary
motor area in startle epilepsy as demonstrated by SEEG
68. Kotagal P, Lüders H, Morris H, Dinner D, Wyllie E, Godoy epileptogenicity maps. Epilepsia 2014; 55(8): e85-8.
J, et al. Dystonic posturing in complex partial seizures of
temporal lobe onset: a new lateralizing sign. Neurology 1989; 86. Werhahn KJ, Noachtar S, Arnold S, Pfänder M, Henkel A,
39(2): 196-201. Winkler PA, et al. Tonic seizures: their significance for
lateralization and frequency in different focal epileptic
69. Marks Jr WJ, Laxer KD. Semiology of temporal lobe syndromes. Epilepsia 2000; 41(9): 1153-61.
seizures: value in lateralizing the seizure focus. Epilepsia
1998; 39(7): 721-6. 87. Chassagnon S, Minotti L, Kremer S, Hoffmann D, Kahane
P. Somatosensory, motor, and reaching/grasping responses
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
70. Yu H-Y, Yiu C-H, Yen D-J, Chen C, Guo Y-C, Kwan S-Y, to direct electrical stimulation of the human cingulate motor
et al. Lateralizing value of early head turning and ictal areas. J Neurosurg 2008; 109(4): 593-604.
dystonia in temporal lobe seizures: a video-EEG study.
Seizure 2001; 10(6): 428-32. 88. Souirti Z, Landré E, Mellerio C, Devaux B, Chassoux F.
Neural network underlying ictal pouting (“chapeau de
71. Dupont S, Semah F, Baulac M, Samson Y. The underlying gendarme”) in frontal lobe epilepsy. Epilepsy Behav 2014;
pathophysiology of ictal dystonia in temporal lobe epilepsy: 37: 249-57.
an FDG-PET study. Neurology 1998; 51(5): 1289-92.
89. Tan Y-L, Muhlhofer W, Knowlton R. Pearls and Oy-
72. Aguglia U, Gambardella A, Piane EL, Messina D, Russo C, sters: The chapeau de gendarme sign and other localizing
Oliveri R, et al. Idiopathic generalized epilepsies with versive gems in frontal lobe epilepsy. Neurology 2016; 87(10):
or circling seizures. Acta Neurol Scand 1999; 99(4): 219-24. e103-5.
73. Dobesberger J, Walser G, Embacher N, Unterberger I, 90. Lu H, Zhang W, Liu S, Sun W. The chapeau de gendarme
Luef G, Bauer G, et al. Gyratory seizures revisited: a video- sign can be evoked by lateral prefrontal epileptic seizures.
EEG study. Neurology 2005; 64(11): 1884-7. Seizure 2021; 87: 17-20.
74. Vercueil L, Kahane P, Francois-Joubert A, Hirsch E, 91. Wiwchar LD, Hader W, Pauranik A, Joseph JT, Appendino
Hoffmann D, Depaulis A, et al. Basal ganglia involvement in JP. Focal seizures associated with the chapeau de gendarme
rotational seizures. Epileptic Disord 1999; 1(2): 107-12. sign or ictal pouting of insular origin. Epilepsy Behav Rep
75. Aguglia U, Gambardella A, Quartarone A, Girlanda P, Le 2019; 12: 100347.
Piane E, Messina D, et al. Interhemispheric threshold 92. Cebeci D, Arhan E, Hirfanoglu T, Karalok ZS, Ercelebi H,
differences in idiopathic generalized epilepsies with versive Dedeoglu Ö, et al. Ictal pouting (‘Chapeau de gendarme’) in
or circling seizures determined with focal magnetic tran- three pediatric cases with cortical dysplasia. Eur J Paediatr
scranial stimulation. Epilepsy Res 2000; 40(1): 1-6. Neurol 2020; 26: 82-8.
76. Gire C, Somma-Mauvais H, Niçaise C, Roussel M, Garnier 93. Rüsch CT, Bölsterli BK, Carosio C, Ramantani G. Chapeau
J-M, Farnarier G. Epileptic nystagmus: electroclinical study of de gendarme in a toddler points to focal epilepsy originating
a case. Epileptic Disord 2001; 3(1): 33-8. from the subcentral gyrus. Epileptic Disord 2021; 23(2): 412-8.
77. Ma Y, Wang J, Li D, Lang S. Two types of isolated epileptic
nystagmus: case report. Int J Clin Exp Med 2015; 8(8): 13500. 94. Ajmone-Marsan CRB. The epileptic seizure: a clinical-
electrographic analysis of Metrazol attacks. Springfield,
78. Globus M, Lavi E, Fich A, Abramsky O. Ictal hemiparesis. Illinois: Thomas, 1957.
Eur Neurol 1982; 21(3): 165-8.
95. Beniczky S, Rubboli G, Covanis A, Sperling MR. Absence-
79. Dale RC, Cross JH. Ictal hemiparesis. Dev Med Child to-bilateral-tonic-clonic seizure: a generalized seizure type.
Neurol 1999; 41(5): 344-7. Neurology 2020; 95(14): e2009-15.
80. Oono M, Uno H, Umesaki A, Nagatsuka K, Kinoshita M, 96. Alexandre V, Mercedes B, Valton L, Maillard L, Bartolo-
Naritomi H. Severe and prolonged ictal paresis in an elderly mei F, Szurhaj W, et al. Risk factors of postictal generalized
patient. Epilepsy Behav Case Rep 2014; 2: 105-7. EEG suppression in generalized convulsive seizures. Neu-
81. Kuba R, J, Brázdil M, Tyrlíková I, Rektor I. rology 2015; 85(18): 1598-603.
Lateralized ictal immobility of the upper limb in patients with 97. Conradsen I, Wolf P, Sams T, Sorensen HB, Beniczky S.
temporal lobe epilepsy. Eur J Neurol 2005; 12(11): 886-90. Patterns of muscle activation during generalized tonic and
82. Maillard L, Gavaret M, Régis J, Wendling F, Bartolomei F. tonic-clonic epileptic seizures. Epilepsia 2011; 52(11):
Fast epileptic discharges associated with ictal negative motor 2125-32.
phenomena. Clin Neurophysiol 2014; 125(12): 2344-8.
98. Kotagal P, Bleasel A, Geller E, Kankirawatana P, Moorjani
83. Pavone P, Polizzi A, Marino SD, Corsello G, Falsaperla R, BI, Rybicki L. Lateralizing value of asymmetric tonic limb
Marino S, et al. West syndrome: a comprehensive review. posturing observed in secondarily generalized tonic-clonic
Neurol Sci 2020; 41(12): 3547-62. seizures. Epilepsia 2000; 41(4): 457-62.
99. Leutmezer F, Wöginger S, Antoni E, Seidl B, Baumgartner but ignored symptom of focal seizures. Epilepsy Behav 2018;
C. Asymmetric ending of secondarily generalized seizures. A 80: 84-9.
lateralizing sign in TLE. Neurology 2002; 59(8): 1252-4.
113. Horinouchi T, Sakurai K, Kurita T, Takeda Y, Yoshida Y,
100. Trinka E, Walser G, Unterberger I, Luef G, Benke T, Akiyama H, et al. Seizure manifesting as a reaching/grasping
Bartha L, et al. Asymmetric termination of secondarily movement in a patient with post-traumatic epilepsy. Clin
generalized tonic-clonic seizures in temporal lobe epilepsy. Case Rep 2018; 6(11): 2271-5.
Neurology 2002; 59(8): 1254-6.
114. Gardella E, Rubboli G, Tassinari CA. Video-EEG analysis
101. Walser G, Unterberger I, Dobesberger J, Embacher N, of ictal repetitive grasping in “frontal-hyperkinetic” seizures.
Falkenstetter T, Larch J, et al. Asymmetric seizure termina- Epileptic Disord 2006; 8(4): 267-73.
tion in primary and secondary generalized tonic-clonic
seizures. Epilepsia 2009; 50(9): 2035-9. 115. Caruana F, Gerbella M, Avanzini P, Gozzo F, Pelliccia V,
Mai R, et al. Motor and emotional behaviours elicited by
102. Wyllie E, Lüders H, Morris HH, Lesser RP, Dinner DS. electrical stimulation of the human cingulate cortex. Brain
The lateralizing significance of versive head and eye 2018; 141(10): 3035-51.
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
105. O’Dwyer R, Silva Cunha JP, Vollmar C, Mauerer C, 119. Asadi-Pooya AA, Wyeth D, Sperling MR. Ictal crying.
Feddersen B, Burgess RC, et al. Lateralizing significance of Epilepsy Behav 2016; 59: 1-3.
quantitative analysis of head movements before secondary 120. Blumberg J, Fernández IS, Vendrame M, Oehl B, Tatum
generalization of seizures of patients with temporal lobe WO, Schuele S, et al. Dacrystic seizures: demographic,
epilepsy. Epilepsia 2007; 48(3): 524-30. semiologic, and etiologic insights from a multicenter study
106. Abarrategui B, Mai R, Sartori I, Francione S, Pelliccia V, in long-term video-EEG monitoring units. Epilepsia 2012; 53
Cossu M, et al. Temporal lobe epilepsy: a never-ending story. (10): 1810-9.
Epilepsy Behav 2021; 122: 108122. 121. Caruana F, Avanzini P, Gozzo F, Francione S, Cardinale
107. Bonini F, McGonigal A, Trébuchon A, Gavaret M, F, Rizzolatti G. Mirth and laughter elicited by electrical
Bartolomei F, Giusiano B, et al. Frontal lobe seizures: from stimulation of the human anterior cingulate cortex. Cortex
clinical semiology to localization. Epilepsia 2014; 55(2): 2015; 71: 323-31.
264-77. 122. Sperli F, Spinelli L, Pollo C, Seeck M. Contralateral smile
108. Tassinari CA, Rubboli G, Gardella E, Cantalupo G, and laughter, but no mirth, induced by electrical stimulation
Calandra-Buonaura G, Vedovello M, et al. Central pattern of the cingulate cortex. Epilepsia 2006; 47(2): 440-3.
generators for a common semiology in fronto-limbic 123. Sturm JW, Andermann F, Berkovic SF. “Pressure to
seizures and in parasomnias. A neuroethologic approach. laugh”: an unusual epileptic symptom associated with small
Neurol Sci 2005; 26(Suppl 3): s225-32. hypothalamic hamartomas. Neurology 2000; 54(4): 971-3.
109. Bartolomei F, Trébuchon A, Gavaret M, Régis J, 124. Hays RS, Lal N, Rosenow J, Macken MP, Schuele SU.
Wendling F, Chauvel P. Acute alteration of emotional Mimetic automatisms expressing a negative affect in two
behaviour in epileptic seizures is related to transient patients with temporal lobe epilepsy. Epilepsy Behav 2011; 20
desynchrony in emotion-regulation networks. Clin Neuro- (3): 572-8.
physiol 2005; 116(10): 2473-9.
125. Tassinari CA, Tassi L, Calandra-Buonaura G, Stanzani-
110. Lee GR, Arain A, Lim N, Lagrange A, Singh P, Abou-Khalil Maserati M, Fini N, Pizza F, et al. Biting behavior, aggression,
B. Rhythmic ictal nonclonic hand (RINCH) motions: a distinct and seizures. Epilepsia 2005; 46(5): 654-63.
contralateral sign in temporal lobe epilepsy. Epilepsia 2006; ·
47(12): 2189-92. 126. Özkara Ç, Taşkıran E, Çarpraz IY, Bilir E, Demir AB, Bora
·
I, et al. Ictal kissing: electroclinical features of an unusual
111. Janszky J, Fogarasi A, Magalova V, Gyimesi C, Kovács N, ictal phenomenon. Seizure 2016; 42: 44-8.
Schulz R, et al. Unilateral hand automatisms in temporal lobe
epilepsy. Seizure 2006; 15(6): 393-6. 127. Guedj E, Guye M, de Laforte C, Chauvel P, Liegeois-
Chauvel C, Mundler O, et al. Neural network underlying ictal
112. Dede H, Bebek N, Gürses C, Baysal-Kıraç L, Baykan B, humming demonstrated by very early SPECT: a case report.
Gökyigit A. Genital automatisms: reappraisal of a remarkable Epilepsia 2006; 47(11): 1968-70.
128. Raghavendra S, Mirsattari S, McLachlan RS. Ictal 144. Maillard L, Vignal JP, Gavaret M, Guye M, Biraben A,
whistling: a rare automatism during temporal lobe seizures. McGonigal A, et al. Semiologic and electrophysiologic
Epileptic Disord 2010; 12(2): 133-5. correlations in temporal lobe seizure subtypes. Epilepsia
2004; 45(12): 1590-9.
129. Rini J, Ochoa J. Mapping musical automatism: further
insights from epileptic high-frequency oscillation analysis. 145. Afif A, Minotti L, Kahane P, Hoffmann D. Anatomofunc-
Neurol Clin Neurosci 2020; 8(4): 177-82. tional organization of the insular cortex: a study using
intracerebral electrical stimulation in epileptic patients.
130. Aupy J, Noviawaty I, Krishnan B, Suwankpakdee P, Epilepsia 2010; 51(11): 2305-15.
Bulacio J, Gonzalez-Martinez J, et al. Insulo-opercular cortex
generates oroalimentary automatisms in temporal seizures. 146. Florindo I, Bisulli F, Pittau F, Naldi I, Striano P, Striano S,
Epilepsia 2018; 59(3): 583-94. et al. Lateralizing value of the auditory aura in partial
seizures. Epilepsia 2006; 47(Suppl 5): 68-72.
131. Wang Y, Wang X, Mo JJ, Sang L, Zhao BT, Zhang C, et al.
Symptomatogenic zone and network of oroalimentary 147. Rona SLH. Auras: localizing and lateralizing value. In:
automatisms in mesial temporal lobe epilepsy. Epilepsia Textbook of epilepsy surgery. CRC Press, 2008.
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
characteristics, seizure spread patterns and results of 175. Mazzola L, Isnard J, Mauguière F. Somatosensory and
surgery. Ann Neurol 1992; 31(1): 3-13. pain responses to stimulation of the second somatosensory
area (SII) in humans. A comparison with SI and insular
160. Jonas J, Rossion B, Brissart H, Frismand S, Jacques C, responses. Cereb Cortex 2006; 16(7): 960-8.
Hossu G, et al. Beyond the core face-processing network:
Intracerebral stimulation of a face-selective area in the right 176. Lim S, Dinner D, Pillay P, Lüders H, Morris H, Klem G,
anterior fusiform gyrus elicits transient prosopagnosia. et al. Functional anatomy of the human supplementary
Cortex 2015; 72: 140-55. sensorimotor area: results of extraoperative electrical
stimulation. Electroencephalogr Clin Neurophysiol 1994; 91
161. Parvizi J, Jacques C, Foster BL, Witthoft N, Rangarajan V, (3): 179-93.
Weiner KS, et al. Electrical stimulation of human fusiform
face-selective regions distorts face perception. J Neurosci 177. Young GB, Blume WT. Painful epileptic seizures. Brain
2012; 32(43): 14915-20. 1983; 106(Pt 3): 537-54.
162. Hausser-Hauw C, Bancaud J. Gustatory hallucinations 178. Mazzola L, Isnard J, Peyron R, Mauguière F. Stimulation
in epileptic seizures. Electrophysiological, clinical and of the human cortex and the experience of pain: wilder
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
anatomical correlates. Brain 1987; 110(Pt 2): 339-59. Penfield’s observations revisited. Brain 2012; 135(Pt 2): 631-40.
163. Mazzola L, Royet JP, Catenoix H, Montavont A, Isnard J, 179. Montavont A, Mauguière F, Mazzola L, Garcia-Larrea L,
Mauguière F. Gustatory and olfactory responses to stimula- Catenoix H, Ryvlin P, et al. On the origin of painful
tion of the human insula. Ann Neurol 2017; 82(3): 360-70. somatosensory seizures. Neurology 2015; 84(6): 594-601.
164. Kanemoto K, Janz D. The temporal sequence of aura- 180. Mauguiere F, Courjon J. Somatosensory epilepsy. A
sensations in patients with complex focal seizures with review of 127 cases. Brain 1978; 101(2): 307-32.
particular attention to ictal aphasia. J Neurol Neurosurg
Psychiatry 1989; 52(1): 52-6. 181. Bernasconi A, Andermann F, Bernasconi N, Reutens DC,
Dubeau F. Lateralizing value of peri-ictal headache: a study of
165. Kim DW, Lee SK, Yun CH, Kim KK, Lee DS, Chung CK, 100 patients with partial epilepsy. Neurology 2001; 56(1): 130-2.
et al. Parietal lobe epilepsy: the semiology, yield of
diagnostic workup and surgical outcome. Epilepsia 2004; 182. Hewett R, Bartolomei F. Epilepsy and the cortical
45(6): 641-9. vestibular system: tales of dizziness and recent concepts.
Front Integr Neurosci 2013; 7: 73.
166. Perven G, So NK. Epileptic auras: phenomenology and
neurophysiology. Epileptic Disord 2015; 17(4): 349-62. 183. Kahane P, Hoffmann D, Minotti L, Berthoz A. Reap-
praisal of the human vestibular cortex by cortical electrical
167. Isnard J, Hagiwara K, Montavont A, Catenoix H, Mazzola stimulation study. Ann Neurol 2003; 54(5): 615-24.
L, Ostrowsky-Coste K, et al. Semiology of insular lobe
seizures. Rev Neurol 2019; 175(3): 144-9. 184. Kun Lee S, Young Lee S, Kim DW, Soo Lee D, Chung CK.
Occipital lobe epilepsy: clinical characteristics, surgical
168. Acharya V, Acharya J, Lüders H. Olfactory epileptic outcome, and role of diagnostic modalities. Epilepsia 2005;
auras. Neurology 1998; 51(1): 56-61. 46(5): 688-95.
169. Kumar G, Juhász C, Sood S, Asano E. Olfactory 185. Blanke O, Landis T, Spinelli L, Seeck M. Out-of-body
hallucinations elicited by electrical stimulation via subdural experience and autoscopy of neurological origin. Brain 2004;
electrodes: effects of direct stimulation of olfactory bulb and 127(2): 243-58.
tract. Epilepsy Behav 2012; 24(2): 264-8.
186. Maillard L, Vignal JP, Anxionnat R, TaillandierVe-
170. Binder DK, Garcia PA, Elangovan GK, Barbaro NM. spignani L. Semiologic value of ictal autoscopy. Epilepsia
Characteristics of auras in patients undergoing temporal 2004; 45(4): 391-4.
lobectomy. J Neurosurg 2009; 111(6): 1283-9.
187. Jonas J, Maillard L, Frismand S, Colnat-Coulbois S,
171. Ferrari-Marinho T, Caboclo LO, Marinho MM, Centeno Vespignani H, Rossion B, et al. Self-face hallucination evoked
RS, Neves RS, Santana MT, et al. Auras in temporal lobe by electrical stimulation of the human brain. Neurology 2014;
epilepsy with hippocampal sclerosis: relation to seizure 83(4): 336-8.
focus laterality and post surgical outcome. Epilepsy Behav
2012; 24(1): 120-5. 188. Arzy S, Seeck M, Ortigue S, Spinelli L, Blanke O.
Induction of an illusory shadow person. Nature 2006; 443
172. Gloor P, Olivier A, Quesney LF, Andermann F, Horowitz (7109): 287.
S. The role of the limbic system in experiential phenomena
of temporal lobe epilepsy. Ann Neurol 1982; 12(2): 129-44. 189. American Psychiatric Association. . Diagnostic and
1
statistical manual of mental disorders (DSM-5 ). American
173. Salanova V, Andermann F, Rasmussen T, Olivier A, Psychiatric Pub, 2013.
Quesney LF. Parietal lobe epilepsy. Clinical manifestations
and outcome in 82 patients treated surgically between 1929 190. Stephani C, Koubeissi M. Hypercognitive seizures
and 1988. Brain 1995; 118(Pt 3): 607-27. – Proposal of a new term for the phenomenon forced
thinking in epilepsy. Epilepsy Res 2017; 134: 63-71.
174. Bartolomei F, Gavaret M, Hewett R, Valton L, Aubert S,
Régis J, et al. Neural networks underlying parietal lobe 191. Mendez MF, Cherrier MM, Perryman KM. Epileptic
seizures: a quantified study from intracerebral recordings. forced thinking from left frontal lesions. Neurology 1996; 47
Epilepsy Res 2011; 93(2-3): 164-76. (1): 79-83.
192. McGonigal A, Chauvel P. Frontal lobe epilepsy: seizure 208. LeDoux JE. Emotion circuits in the brain. Annu Rev
semiology and presurgical evaluation. Pract Neurol 2004; 4 Neurosci 2000; 23: 155-84.
(5): 260-73.
209. Young GB, Chandarana PC, Blume WT, McLachlan RS,
193. Johanson M, Valli K, Revonsuo A, Wedlund JE. Content Muñoz DG, Girvin JP. Mesial temporal lobe seizures
analysis of subjective experiences in partial epileptic presenting as anxiety disorders. J Neuropsychiatry Clin
seizures. Epilepsy Behav 2008; 12(1): 170-82. Neurosci 1995; 7(3): 352-7.
194. Yih J, Beam DE, Fox KC, Parvizi J. Intensity of affective 210. Hingray C, McGonigal A, Kotwas I, Micoulaud-Franchi
experience is modulated by magnitude of intracranial JA. The relationship between epilepsy and anxiety disorders.
electrical stimulation in human orbitofrontal, cingulate Curr Psychiatry Rep 2019; 21(6): 40.
and insular cortices. Soc Cogn Affect Neurosci 2019; 14(4):
339-51. 211. Hurley RA, Fisher R, Taber KH. Sudden onset panic:
epileptic aura or panic disorder? J Neuropsychiatry Clin
195. Fournier NM, Brandt LE, Kalynchuk LE. The effect of left Neurosci 2006; 18(4): 436-43.
and right long-term amygdala kindling on interictal emo-
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
tionality and Fos expression. Epilepsy Behav 2020; 104(Pt A): 212. Gloor P. Experiential phenomena of temporal lobe
106910. epilepsy. Facts and hypotheses. Brain 1990; 113(Pt 6): 1673-94.
196. Fox KCR, Yih J, Raccah O, Pendekanti SL, Limbach LE, 213. Mula M. Epilepsy-induced behavioral changes during
Maydan DD, et al. Changes in subjective experience elicited the ictal phase. Epilepsy Behav 2014; 30: 14-6.
by direct stimulation of the human orbitofrontal cortex. 214. Guimond A, Braun CM, Bélanger E, Rouleau I. Ictal fear
Neurology 2018; 91(16): e1519-27. depends on the cerebral laterality of the epileptic activity.
197. Toth V, Fogarasi A, Karadi K, Kovacs N, Ebner A, Janszky Epileptic Disord 2008; 10(2): 101-12.
J. Ictal affective symptoms in temporal lobe epilepsy are 215. Labudda K, Mertens M, Steinkroeger C, Bien CG,
related to gender and age. Epilepsia 2010; 51(7): 1126-32. Woermann FG. Lesion side matters – an fMRI study on the
198. Mathiak KA, Mathiak K, Wolańczyk T, Ostaszewski P. association between neural correlates of watching dynamic
Psychosocial impairments in children with epilepsy depend fearful faces and their evaluation in patients with temporal
on the side of the focus. Epilepsy Behav 2009; 16(4): 603-8. lobe epilepsy. Epilepsy Behav 2014; 31: 321-8.
199. LaBar KS, LeDoux JE, Spencer DD, Phelps EA. Impaired 216. Urbanic PT, Zaar K, Eder H, Gruber-Cichocky L,
fear conditioning following unilateral temporal lobectomy Feichtinger M. Ictal fear auras after selective amygdalohip-
in humans. J Neurosci 1995; 15(10): 6846-55. pocampectomy: the use of ictal SPECT and scalp EEG in the
presurgical reevaluation. Epilepsy Behav 2011; 22(3): 577-80.
200. van Elst LT, Woermann FG, Lemieux L, Thompson PJ, 217. Gläscher J, Adolphs R. Processing of the arousal of
Trimble MR. Affective aggression in patients with temporal subliminal and supraliminal emotional stimuli by the human
lobe epilepsy: a quantitative MRI study of the amygdala. amygdala. J Neurosci 2003; 23(32): 10274-82.
Brain 2000; 123(Pt 2): 234-43.
218. Manford M, Fish DR, Shorvon SD. An analysis of clinical
201. Davidson RJ, Putnam KM, Larson CL. Dysfunction in the seizure patterns and their localizing value in frontal and
neural circuitry of emotion regulation – a possible prelude temporal lobe epilepsies. Brain 1996; 119(Pt 1): 17-40.
to violence. Science 2000; 289(5479): 591-4.
219. Biraben A, Taussig D, Thomas P, Even C, Vignal JP,
202. Saleh C, Reuber M, Beyenburg S. Epileptic seizures and Scarabin JM, et al. Fear as the main feature of epileptic
criminal acts: is there a relationship? Epilepsy Behav 2019; 97: seizures. J Neurol Neurosurg Psychiatry 2001; 70(2): 186-91.
15-21.
220. Nair PP, Menon RN, Radhakrishnan A, Cherian A,
203. Saegusa S, Takahashi T, Moriya J, Yamakawa J, Itoh T, Abraham M, Vilanilam G, et al. Is ’burned-out hippocampus’
Kusaka K, et al. Panic attack symptoms in a patient with left syndrome a distinct electro-clinical variant of MTLE-HS
temporal lobe epilepsy. J Int Med Res 2004; 32(1): 94-6. syndrome? Epilepsy Behav 2017; 69: 53-8.
204. Sazgar M, Carlen PL, Wennberg R. Panic attack 221. Meletti S, Tassi L, Mai R, Fini N, Tassinari CA, Russo GL.
semiology in right temporal lobe epilepsy. Epileptic Disord Emotions induced by intracerebral electrical stimulation of
2003; 5(2): 93-100. the temporal lobe. Epilepsia 2006; 47(Suppl 5): 47-51.
205. Bartolomeil F, Guye M, Wendling F, Gavaret M, Régis J, 222. Chang CN, Ojemann LM, Ojemann GA, Lettich E.
Chauvel P. Fear, anger and compulsive behavior during Seizures of fronto-orbital origin: a proven case. Epilepsia
seizure: involvement of large scale fronto-temporal neural 1991; 32(4): 487-91.
networks. Epileptic Disord 2002; 4(4): 235-41.
223. Alkawadri R, So NK, Van Ness PC, Alexopoulos AV.
206. Altshuler LL, Devinsky O, Post RM, Theodore W. Cingulate epilepsy: report of 3 electroclinical subtypes with
Depression, anxiety, and temporal lobe epilepsy. Laterality surgical outcomes. JAMA Neurol 2013; 70(8): 995-1002.
of focus and symptoms. Arch Neurol 1990; 47(3): 284-8.
224. Wang J, Wang Q, Wang M, Luan G, Zhou J, Guan Y, et al.
207. Devinsky O, Barr WB, Vickrey BG, Berg AT, Bazil CW, Occipital lobe epilepsy with ictal fear: evidence from a
Pacia SV, et al. Changes in depression and anxiety after stereo-electroencephalography (sEEG) case. Front Neurol
resective surgery for epilepsy. Neurology 2005; 65(11): 1744-9. 2018; 9: 644.
225. Oehl B, Schulze-Bonhage A, Lanz M, Brandt A, 243. Cabrera-Valdivia F, Jiménez-Jiménez FJ, Tejeiro J,
Altenmüller DM. Occipital lobe epilepsy with fear as leading Ayuso-Peralta L, Vaquero A, Garcia-Albea E. Dostoevsky’s
ictal symptom. Epilepsy Behav 2012; 23(3): 379-83. epilepsy induced by television. J Neurol Neurosurg Psychia-
try 1996; 61(6): 653.
226. Nitta N, Usui N, Kondo A, Tottori T, Terada K, Araki Y,
et al. Semiology of hyperkinetic seizures of frontal versus 244. Dolgoff-Kaspar R, Ettinger AB, Golub SA, Perrine K,
temporal lobe origin. Epileptic Disord 2019; 21(2): 154-65. Harden C, Croll SD. Numinous-like auras and spirituality in
persons with partial seizures. Epilepsia 2011; 52(3): 640-4.
227. Williams D. The structure of emotions reflected in
epileptic experiences. Brain 1956; 79(1): 29-67. 245. Saver JL, Rabin J. The neural substrates of religious
experience. J Neuropsychiatry Clin Neurosci 1997; 9(3):
228. Singh TD, Sabsevitz DS, Desai NN, Middlebrooks EH, 498-510.
Feyissa AM, Grewal S, et al. Crying with depressed affect
induced by electrical stimulation of the anterior insula: a 246. Devinsky O, Lai G. Spirituality and religion in epilepsy.
stereo EEG case study. Epilepsy Behav Rep 2021; 15: 100421. Epilepsy Behav 2008; 12(4): 636-43.
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
229. ILAE. Emotional seizures. www.epilepsydiagnosis.org 247. Janszky J, Ebner A, Szupera Z, Schulz R, Hollo A, Szücs
[6/30/2021]. A, et al. Orgasmic aura – a report of seven cases. Seizure
2004; 13(6): 441-4.
230. Perini G, Mendius R. Depression and anxiety in
complex partial seizures. J Nerv Ment Dis 1984; 172(5): 287-90. 248. Aull-Watschinger S, Pataraia E, Baumgartner C. Sexual
auras: predominance of epileptic activity within the mesial
231. Bartolomei F, Lagarde S, Scavarda D, Carron R, Bénar temporal lobe. Epilepsy Behav 2008; 12(1): 124-7.
CG, Picard F. The role of the dorsal anterior insula in ecstatic
sensation revealed by direct electrical brain stimulation. 249. Remillard GM, Andermann F, Testa GF, Gloor P, Aube
Brain Stimul 2019; 12(5): 1121-6. M, Martin JB, et al. Sexual ictal manifestations predominate
in women with temporal lobe epilepsy: a finding suggesting
232. Carrazana E, Cheng J. St Theresa’s dart and a case of sexual dimorphism in the human brain. Neurology 1983; 33
religious ecstatic epilepsy. Cogn Behav Neurol 2011; 24(3): (3): 323-30.
152-5.
250. Spencer SS, Spencer DD, Williamson PD, Mattson RH.
233. Asheim Hansen B, Brodtkorb E. Partial epilepsy with Sexual automatisms in complex partial seizures. Neurology
“ecstatic” seizures. Epilepsy Behav 2003; 4(6): 667-73. 1983; 33(5): 527-33.
234. Gschwind M, Picard F. Ecstatic epileptic seizures: a 251. Felician O, Tramoni E, Bartolomei F. Transient epileptic
glimpse into the multiple roles of the insula. Front Behav amnesia: update on a slowly emerging epileptic syndrome.
Neurosci 2016; 10: 21. Rev Neurol (Paris) 2015; 171(3): 289-97.
235. Picard F, Craig AD. Ecstatic epileptic seizures: a 252. Heydrich L, Marillier G, Evans N, Seeck M, Blanke O.
potential window on the neural basis for human self- Depersonalization- and derealization-like phenomena of
awareness. Epilepsy Behav 2009; 16(3): 539-46. epileptic origin. Ann Clin Transl Neurol 2019; 6(9): 1739-47.
236. Picard F, Kurth F. Ictal alterations of consciousness 253. Trebuchon A, Lambert I, Guisiano B, McGonigal A,
during ecstatic seizures. Epilepsy Behav 2014; 30: 58-61. Perot C, Bonini F, et al. The different patterns of seizure-
237. Meyer GMM, Martin W, McGraw CP. Stereotactic induced aphasia in temporal lobe epilepsies. Epilepsy Behav
cingulotomy with results of acute stimulation and serial 2018; 78: 256-64.
psychological testing. In : Laitinen LV, ed. Surgical
approaches in psychiatry. Lancaster (UK): Baltimore: 39-58. 254. Loesch AM, Steger H, Losher C, Hartl E, Rémi J, Vollmar
C, et al. Seizure-associated aphasia has good lateralizing but
238. Talairach J, Bancaud J, Geier S, Bordas-Ferrer M, poor localizing significance. Epilepsia 2017; 58(9): 1551-5.
Bonis A, Szikla G, et al. The cingulate gyrus and human
behaviour. Electroencephalogr Clin Neurophysiol 1973; 34 255. Eggleston KS, Olin BD, Fisher RS. Ictal tachycardia: the
(1): 45-52. head-heart connection. Seizure 2014; 23(7): 496-505.
239. Penfield WKK. Epileptic seizure patterns: a study of the 256. Garcia M, D’Giano C, Estellés S, Leiguarda R, Rabino-
localizing value of initial phenomena in focal cortical wicz A. Ictal tachycardia: its discriminating potential
seizures. Springfield, Illinois: Thomas, 1951. between temporal and extratemporal seizure foci. Seizure
2001; 10(6): 415-9.
240. Vera CL, Patel SJ, Naso W. “Dual pathology” and the
significance of surgical outcome in “Dostoewsky’s epilep- 257. Weil S, Arnold S, Eisensehr I, Noachtar S. Heart rate
sy”. Epileptic Disord 2000; 2(1): 21-5. increase in otherwise subclinical seizures is different in
temporal versus extratemporal seizure onset: support for
241. Stefan H, Schulze-Bonhage A, Pauli E, Platsch G, Quiske temporal lobe autonomic influence. Epileptic Disord 2005; 7
A, Buchfelder M, et al. Ictal pleasant sensations: (3): 199-204.
cerebral localization and lateralization. Epilepsia 2004; 45
(1): 35-40. 258. Pavlova M, Abdennadher M, Singh K, Katz E, Llewellyn
N, Zarowsky M, et al. Advantages of respiratory monitoring
242. Roodakker KR, Ezra B, Gauffin H, Latini F, Zetterling M, during video-EEG evaluation to differentiate epileptic
Berntsson S, et al. Ecstatic and gelastic seizures relate to the seizures from other events. Epilepsy Behav 2014; 32:
hypothalamus. Epilepsy Behav Rep 2020; 14: 100358. 142-4.
259. Moseley BD, Wirrell EC, Nickels K, Johnson JN, Acker- 275. Ghearing GR, Munger TM, Jaffe AS, Benarroch EE,
man MJ, Britton J. Electrocardiographic and oximetric Britton JW. Clinical cues for detecting ictal asystole. Clin
changes during partial complex and generalized seizures. Auton Res 2007; 17(4): 221-6.
Epilepsy Res 2011; 95(3): 237-45.
276. Van Buren JM. The abdominal aura. A study of
260. Jaychandran R, Chaitanya G, Satishchandra P, Bharath abdominal sensations occurring in epilepsy and produced
RD, Thennarasu K, Sinha S. Monitoring peri-ictal changes in by depth stimulation. Electroencephalogr Clin Neurophysiol
heart rate variability, oxygen saturation and blood pressure 1963; 15: 1-19.
in epilepsy monitoring unit. Epilepsy Res 2016; 125: 10-8.
277. Mulder DW, Daly D, Bailey AA. Visceral epilepsy. AMA
261. van der Lende M, Arends JB, Lamberts RJ, Tan HL, de Arch Intern Med 1954; 93(4): 481-93.
Lange FJ, Sander JW, et al. The yield of long-term
electrocardiographic recordings in refractory focal epilepsy. 278. Specchio N, Trivisano M, Di Ciommo V, Cappelletti S,
Epilepsia 2019; 60(11): 2215-23. Masciarelli G, Volkov J, et al. Panayiotopoulos syndrome: a
clinical, EEG, and neuropsychological study of 93 consecu-
262. Walker F, Fish DR. Recording respiratory parameters in tive patients. Epilepsia 2010; 51(10): 2098-107.
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
291. Stefan H, Feichtinger M, Black A. Autonomic pheno- 307. Musilová K, Kuba R, Brázdil M, Tyrlíková I, Rektor I.
mena of temperature regulation in temporal lobe epilepsy. Occurrence and lateralizing value of “rare” peri-ictal
Epilepsy Behav 2003; 4(1): 65-9. vegetative symptoms in temporal lobe epilepsy. Epilepsy
Behav 2010; 19(3): 372-5.
292. Stefan H, Pauli E, Kerling F, Schwarz A, Koebnick C.
Autonomic auras: left hemispheric predominance of epilep- 308. Voss NF, Davies KG, Boop FA, Montouris GD, Hermann
tic generators of cold shivers and goose bumps? Epilepsia BP. Spitting automatism in complex partial seizures: a
2002; 43(1): 41-5. nondominant temporal localizing sign? Epilepsia 1999; 40
(1): 114-6.
293. Tényi D, Bóné B, Horváth R, Komoly S, Illés Z, Beier CP,
et al. Ictal piloerection is associated with high-grade glioma 309. Vojvodic N, Ristic AJ, Bascarevic V, Popovic L, Parojcic A,
and autoimmune encephalitis – Results from a systematic Koprivsek K, et al. Ictal spitting in left temporal lobe epilepsy
review. Seizure 2019; 64: 1-5. and fMRI speech lateralization. Clin Neurol Neurosurg 2013;
115(4): 495-7.
294. Baysal-Kirac L, Tuzun E, Erdag E, Ulusoy C, Vanli-Yavuz
EN, Ekizoglu E, et al. Neuronal autoantibodies in epilepsy 310. Kellinghaus C, Loddenkemper T, Kotagal P. Ictal
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
patients with peri-ictal autonomic findings. J Neurology 2016; spitting: clinical and electroencephalographic features.
263(3): 455-66. Epilepsia 2003; 44(8): 1064-9.
295. Baumgartner C, Lurger S, Leutmezer F. Autonomic 311. Quevedo-Diaz M, Campo AT, Vila-Vidal M, Principe A,
symptoms during epileptic seizures. Epileptic Disord 2001; 3 Ley M, Rocamora R. Ictal spitting in non-dominant temporal
(3): 103-16. lobe epilepsy: an anatomo-electrophysiological correlation.
Epileptic Disord 2018; 20(2): 139-45.
296. Janszky J, Fogarasi A, Toth V, Magalova V, Gyimesi C,
Kovacs N, et al. Peri-ictal vegetative symptoms in temporal 312. Park S-M, Lee S-A, Kim JH, Kang JK. Ictal spitting in a
lobe epilepsy. Epilepsy Behav 2007; 11(1): 125-9. patient with dominant temporal lobe epilepsy: supporting
evidence of ictal spitting from the nondominant hemi-
297. Henkel A, Noachtar S, Pfänder M, Lüders HO. sphere. Eur Neurol 2007; 57(1): 47.
The localizing value of the abdominal aura and its
evolution: a study in focal epilepsies. Neurology 2002; 58 313. Özkara C, Hanoglu L, Eskazan E, Kulaksizogvlu IB,
(2): 271-6. Özyurt E. Ictal spitting during a left emporal lobe-originated
complex partial seizure: a case report. Epileptic Disord 2000;
298. Gil-Nagel A, Risinger MW. Ictal semiology in hippo- 2(3): 169-72.
campal versus extrahippocampal temporal lobe epilepsy.
Brain 1997; 120(1): 183-92. 314. Caboclo LOSF, Miyashira FS, Hamad APA, Lin K, Carrete
Jr H, Sakamoto AC, et al. Ictal spitting in left temporal lobe
299. Gupta A, Jeavons P, Hughes R, Covanis A. Aura in epilepsy: report of three cases. Seizure 2006; 15(6): 462-7.
temporal lobe epilepsy: clinical and electroencephalograph-
ic correlation. J Neurol Neurosurg Psychiatry 1983; 46(12): 315. Fiol ME, Leppik IE, Mireles R, Maxwell R. Ictus emeticus
1079-83. and the insular cortex. Epilepsy Res 1988; 2(2): 127-31.
300. Taylor DC, Lochery M. Temporal lobe epilepsy: origin 316. Kramer RE, Lüders H, Goldstick L, Dinner D, Morris H,
and significance of simple and complex auras. J Neurol Lesser R, et al. Ictus emeticus: an electroclinical analysis.
Neurosurg Psychiatry 1987; 50(6): 673-81. Neurology 1988; 38(7): 1048-52.
301. Palmini A, Gloor P. The localizing value of auras in 317. Guerrini R, Ferrari A, Battaglia A, Salvadori P, Bonanni P.
partial seizures: a prospective and retrospective study. Occipitotemporal seizures with ictus emeticus induced by
Neurology 1992; 42(4): 801-8. intermittent photic stimulation. Neurology 1994; 44(2): 253-9.
302. Fried I, Spencer DD, Spencer SS. The anatomy of 318. Devinsky O, Frasca J, Pacia S, Luciano D, Paraiso J, Doyle
epileptic auras: focal pathology and surgical outcome. J W. Ictus emeticus: further evidence of nondominant
Neurosurg 1995; 83(1): 60-6. temporal involvement. Neurology 1995; 45(6): 1158-60.
303. Shah J, Zhai H, Fuerst D, Watson C. Hypersalivation in 319. Kotagal P, Lüders HO, Williams G, Nichols TR,
temporal lobe epilepsy. Epilepsia 2006; 47(3): 644-51. McPherson J. Psychomotor seizures of temporal lobe onset:
analysis of symptom clusters and sequences. Epilepsy Res
304. Hoffmann JM, Elger CE, Kleefuss-Lie AA. The localizing 1995; 20(1): 49-67.
value of hypersalivation and postictal coughing in temporal
lobe epilepsy. Epilepsy Res 2009; 87(2-3): 144-7. 320. Baumgartner C, Olbrich A, Lindinger G, Pataraia E,
Gröppel G, Bacher J, et al. Regional cerebral blood flow
305. Satow T, Ikeda A, Hayashi N, Yamamoto J, Takayama M, during temporal lobe seizures associated with ictal vomiting:
Matsuhashi M, et al. Surgical treatment of seizures from an ictal SPECT study in two patients. Epilepsia 1999; 40(8):
the peri-Sylvian area by perinatal insult: a case report 1085-91.
of ictal hypersalivation. Acta Neurochir 2004; 146(9):
1021-6. 321. Chen C, Yen D-J, Yiu C-H, Shih Y-H, Yu H-Y, Su M-S.
Ictal vomiting in partial seizures of temporal lobe origin. Eur
306. Proserpio P, Cossu M, Francione S, Tassi L, Mai R, Neurol 1999; 42(4): 235-9.
Didato G, et al. Insular-opercular seizures manifesting with
sleep-related paroxysmal motor behaviors: a stereo-EEG 322. Schäuble B, Britton JW, Mullan BP, Watson J, Shar-
study. Epilepsia 2011; 52(10): 1781-91. brough FW, Marsh WR. Ictal vomiting in association with left
temporal lobe seizures in a left hemisphere language- 340. Rathore G, Larsen P, Parakh M, Fernandez C. Choking at
dominant patient. Epilepsia 2002; 43(11): 1432-5. night: a case of opercular nocturnal frontal lobe epilepsy.
Case Rep Pediatr 2013; 2013: 606385.
323. Schindler K, Wieser HG. Ictal vomiting in a left
hemisphere language-dominant patient with left-sided 341. Davis KA, Cantor C, Maus D, Herman ST. A neurological
temporal lobe epilepsy. Epilepsy Behav 2006; 8(1): 323-7. cause of recurrent choking during sleep. J Clin Sleep Med
2008; 4(6): 586-7.
324. Tarnutzer AA, Mothersill I, Imbach LL. Ictal nausea and
vomiting – Is it left or right? Seizure 2018; 61: 83-8. 342. Geevasinga N, Archer JS, Ng K. Choking, asphyxiation
and the insular seizure. J Clin Neurosci 2014; 21(4):
325. Pietrafusa N, de Palma L, De Benedictis A, Trivisano M, 688-9.
Marras CE, Vigevano F, et al. Ictal vomiting as a sign of
temporal lobe epilepsy confirmed by stereo-EEG and 343. Isnard J, Guénot M, Sindou M, Mauguière F. Clinical
surgical outcome. Epilepsy Behav 2015; 53: 112-6. manifestations of insular lobe seizures: a stereo-electroen-
cephalographic study. Epilepsia 2004; 45(9): 1079-90.
326. Catenoix H, Isnard J, Guénot M, Petit J, Remy C,
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
Mauguière F. The role of the anterior insular cortex in ictal 344. O’Regan ME, Brown JK. Abnormalities in cardiac and
vomiting: a stereotactic electroencephalography study. respiratory function observed during seizures in childhood.
Epilepsy Behav 2008; 13(3): 560-3. Dev Med Child Neurol 2005; 47(1): 4-9.
327. Strzelczyk A, Nowak M, Bauer S, Reif PS, Oertel WH, 345. Singh K, Katz ES, Zarowski M, Loddenkemper T,
Knake S, et al. Localizing and lateralizing value of ictal Llewellyn N, Manganaro S, et al. Cardiopulmonary compli-
flatulence. Epilepsy Behav 2010; 17(2): 278-82. cations during pediatric seizures: a prelude to understand-
ing SUDEP. Epilepsia 2013; 54(6): 1083-91.
328. Vittal NB, Singh P, Azar NJ. Ictal flatulence: seizure
onset in the nondominant hemisphere. Epilepsy Behav 2009; 346. Pavlova M, Singh K, Abdennadher M, Katz ES, Dwor-
16(4): 663-5. etzky BA, White DP, et al. Comparison of cardiorespiratory
and EEG abnormalities with seizures in adults and children.
329. Koubeissi MZ, Crone NE, Lesser RP. Seizures manifest- Epilepsy Behav 2013; 29(3): 537-41.
ing as an urge to defecate, with an ictal discharge in the right
hemisphere. Epilepsia 2005; 46(8): 1330-2. 347. Foldvary N, Lee N, Thwaites G, Mascha E, Hammel J, Kim
H, et al. Clinical and electrographic manifestations of
330. Taieb G, Renard D, Labauge P, Janicot F, Briere C. Ictal lesional neocortical temporal lobe epilepsy. Neurology
urge to defecate associated with a right-sided mesial 1997; 49(3): 757-63.
temporal cavernoma. Epilepsy Behav 2012; 24(2): 272-3.
348. Harvey AS, Hopkins IJ, Bowe JM, Cook DJ, Shield LK,
331. Mestre TA, Bentes C, Pimentel J. Ictal eructation: a case Berkovic SF. Frontal lobe epilepsy: clinical seizure char-
report. Epileptic Disord 2008; 10(2): 170-2. acteristics and localization with ictal 99mTc-HMPAO SPECT.
332. Bateman LM, Li CS, Seyal M. Ictal hypoxemia in Neurology 1993; 43(10): 1966-80.
localization-related epilepsy: analysis of incidence, severity 349. Freeman R, Schachter SC. Autonomic epilepsy. Semin
and risk factors. Brain 2008; 131(Pt 12): 3239-45. Neurol 1995; 15(2): 158-66.
333. Lacuey N, Zonjy B, Hampson JP, Rani MRS, Zaremba A,
Sainju RK, et al. The incidence and significance of periictal 350. Shahar E, Andraus J. Near reflex accommodation spasm:
apnea in epileptic seizures. Epilepsia 2018; 59(3): 573-82. unusual presentation of generalized photosensitive epilep-
sy. J Clin Neurosci 2002; 9(5): 605-7.
334. Singh B, Al Shahwan A, Al Deeb SM. Partial seizures
presenting as life-threatening apnea. Epilepsia 1993; 34(5): 351. Rosenberg ML, Jabbari B. Miosis and internal ophthal-
901-3. moplegia as a manifestation of partial seizures. Neurology
1991; 41(5): 737-9.
335. Seyal M, Bateman LM. Ictal apnea linked to contralateral
spread of temporal lobe seizures: intracranial EEG record- 352. Sadek AR, Kirkham F, Barker S, Gray WP, Allen D.
ings in refractory temporal lobe epilepsy. Epilepsia 2009; 50 Seizure-induced miosis. Epilepsia 2011; 52(12): e199-203.
(12): 2557-62.
353. Afifi AK, Corbett JJ, Thompson HS, Wells KK. Seizure-
336. Tio E, Culler GW, Bachman EM, Schuele S. Ictal central induced miosis and ptosis: association with temporal lobe
apneas in temporal lobe epilepsies. Epilepsy Behav 2020; 112: magnetic resonance imaging abnormalities. J Child Neurol
107434. 1990; 5(2): 142-6.
337. Lacuey N, Hupp NJ, Hampson J, Lhatoo S. Ictal Central 354. Lance JW, Smee RI. Partial seizures with visual
Apnea (ICA) may be a useful semiological sign in invasive disturbance treated by radiotherapy of cavernous hemangi-
epilepsy surgery evaluations. Epilepsy Res 2019; 156: 106164. oma. Ann Neurol 1989; 26(6): 782-5.
338. Cohen HA, Ashkenazi A, Barzilai A, Lahat E. Nocturnal 355. Tamburin S, Turri G, Kuhdari P, Fiaschi A, Manganotti P.
acute laryngospasm in children: a possible epileptic Unilateral fixed mydriasis: an uncommon presentation of
phenomenon. J Child Neurol 2000; 15(3): 202-4. temporal lobe epilepsy. J Neurol 2012; 259(2): 355-7.
339. Oldani A, Zucconi M, Castronovo C, Ferini-Strambi L. 356. Masjuan J, García-Segovia J, Barón M, Alvarez-Cermeño
Nocturnal frontal lobe epilepsy misdiagnosed as sleep JC. Ipsilateral mydriasis in focal occipitotemporal seizures. J
apnea syndrome. Acta Neurol Scand 1998; 98(1): 67-71. Neurol Neurosurg Psychiatry 1997; 63(6): 810-1.
357. Gadoth N, Margalith D, Bechar M. Unilateral pupillary 373. Kellinghaus C, Kotagal P. Lateralizing value of Todd’s
dilatation during focal seizures. J Neurol 1981; 225(3): palsy in patients with epilepsy. Neurology 2004; 62(2):
227-30. 289-91.
358. Loddenkemper T, Foldvary N, Raja S, Neme S, Lüders 374. Leutmezer F, Baumgartner C. Postictal signs of later-
HO. Ictal urinary urge: further evidence for lateralization alizing and localizing significance. Epileptic Disord 2002; 4(1):
to the nondominant hemisphere. Epilepsia 2003; 44(1): 43-8.
124-6.
375. Werhahn KJ. Weakness and focal sensory deficits in the
359. Gurgenashvili K, Massey SL, Grant M, Piatt Jr J, Legido A, postictal state. Epilepsy Behav 2010; 19(2): 138-9.
Valencia I. Intracranial localisation of ictal urinary urge
epileptogenic zone to the non-dominant temporal lobe. 376. Kosnik E, Paulson GW, Laguna JF. Postictal blindness.
Epileptic Disord 2011; 13(4): 430-4. Neurology 1976; 26(3): 248-50.
360. Yilmaz S, Gokben S, Turhan T, Serdaroglu G, Tekgul H. 377. Hadjikoutis S, Sawhney IM. Occipital seizures present-
Ictal urinary urge: localization and lateralization value in a ing with bilateral visual loss. Neurol India 2003; 51(1):
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
361. Dobesberger J, Walser G, Unterberger I, Embacher N, 378. Caraballo R, Koutroumanidis M, Panayiotopoulos CP,
Luef G, Bauer G, et al. Genital automatisms: a video-EEG Fejerman N. Idiopathic childhood occipital epilepsy of
study in patients with medically refractory seizures. Epilepsia Gastaut: a review and differentiation from migraine and
2004; 45(7): 777-80. other epilepsies. J Child Neurol 2009; 24(12): 1536-42.
362. Stoffels C, Munari C, Bonis A, Bancaud J, Talairach J. 379. Salmon JH. Transient postictal hemianopsia. Arch
Genital and sexual manifestations occurring in the course of Ophthalmol 1968; 79(5): 523-5.
partial seizures in man (author’s transl.). Rev Electroence- 380. Privitera M, Kim KK. Postictal language function.
phalogr Neurophysiol Clin 1980; 10(4): 386-92. Epilepsy Behav 2010; 19(2): 140-5.
363. Kasper BS, Kerling F, Graf W, Stefan H, Pauli E. Ictal 381. Leutmezer F, Serles W, Lehrner J, Pataraia E, Zeiler K,
delusion of sexual transformation. Epilepsy Behav 2009; 16 Baumgartner C. Postictal nose wiping: a lateralizing sign in
(2): 356-9. temporal lobe complex partial seizures. Neurology 1998; 51
364. Fisher RS, Schachter SC. The postictal state: a neglected (4): 1175-7.
entity in the management of epilepsy. Epilepsy Behav 2000; 1 382. Geyer JD, Payne TA, Faught E, Drury I. Postictal nose-
(1): 52-9. rubbing in the diagnosis, lateralization, and localization of
365. Engel JJ. Seizures and epilepsy. Philadelphia: F.A. Davis seizures. Neurology 1999; 52(4): 743-5.
Company, 1989. 383. Hirsch LJ, Lain AH, Walczak TS. Postictal nosewiping
366. Ryvlin P, Nashef L, Lhatoo SD, Bateman LM, Bird J, lateralizes and localizes to the ipsilateral temporal lobe.
Bleasel A, et al. Incidence and mechanisms of cardiorespira- Epilepsia 1998; 39(9): 991-7.
tory arrests in epilepsy monitoring units (MORTEMUS): a 384. Wennberg R. Electroclinical analysis of postictal noser-
retrospective study. Lancet Neurol 2013; 12(10): 966-77. ubbing. Can J Neurol Sci 2000; 27(2): 131-6.
367. Subota A, Khan S, Josephson CB, Manji S, Lukmanji S, 385. Çilliler AE, Güven H, Çomoglu SS. Epilepsy and
Roach P, et al. Signs and symptoms of the postictal period in headaches: further evidence of a link. Epilepsy Behav
epilepsy: A systematic review and meta-analysis. Epilepsy 2017; 70(Pt A): 161-5.
Behav 2019; 94: 243-51.
386. Ekstein D, Schachter SC. Postictal headache. Epilepsy
368. Pottkämper JCM, Hofmeijer J, van Waarde JA, van Behav 2010; 19(2): 151-5.
Putten M. The postictal state – What do we know? Epilepsia
2020; 61(6): 1045-61. 387. Yankovsky AE, Andermann F, Bernasconi A. Character-
istics of headache associated with intractable partial epilep-
369. Rolak LA, Rutecki P, Ashizawa T, Harati Y. Clinical sy. Epilepsia 2005; 46(8): 1241-5.
features of Todd’s post-epileptic paralysis. J Neurol Neuro-
surg Psychiatry 1992; 55(1): 63-4. 388. Ito M, Schachter SC. Frequency and characteristics of
interictal headaches in patients with epilepsy. J Epilepsy
370. Leutmezer F, Serles W, Pataraia E, Olbrich A, Bacher J, 1996; 9(2): 83-6.
Aull S, et al. The postictal state. A clinically oriented
observation of patients with epilepsy. Wien Klin Wochenschr 389. Mohamed W, Ahuja N, Shah A. Palinacousis – evidence
1998; 110(11): 401-7. to suggest a post-ictal phenomenon. J Neurol Sci 2012; 317(1-
2): 6-12.
371. Adam C, Adam C, Rouleau I, Saint-Hilaire JM. Postictal
aphasia and paresis: a clinical and intracerebral EEG study. 390. Simon RP. Heart and lung in the postictal state. Epilepsy
Can J Neurol Sci 2000; 27(1): 49-54. Behav 2010; 19(2): 167-71.
372. Gallmetzer P, Leutmezer F, Serles W, Assem-Hilger E, 391. Fauser S, Wuwer Y, Gierschner C, Schulze-Bonhage A.
Spatt J, Baumgartner C. Postictal paresis in focal epilepsies The localizing and lateralizing value of ictal/postictal
– incidence, duration, and causes: a video-EEG monitoring coughing in patients with focal epilepsies. Seizure 2004; 13
study. Neurology 2004; 62(12): 2160-4. (6): 403-10.
392. Azar NJ, Tayah TF, Wang L, Song Y, Abou-Khalil BW. of caspr2 antibody-associated autoimmune encephalitis.
Postictal breathing pattern distinguishes epileptic from Epileptic Disord 2014; 16(4): 477-81.
nonepileptic convulsive seizures. Epilepsia 2008; 49(1): 132-7.
410. Lüders H, Vaca GF, Akamatsu N, Amina S, Arzimanoglou
393. Oueslati B, Fekih-Romdhane F, Ridha R. Postictal A, Baumgartner C, et al. Classification of paroxysmal events
delirium and violent behavior in patients with post- and the four-dimensional epilepsy classification system.
neurosurgical epilepsy. World Neurosurg 2018; 115: 193-5. Epileptic Disord 2019; 21(1): 1-29.
394. Clancy MJ, Clarke MC, Connor DJ, Cannon M, Cotter 411. Varley J, Wehner T, Sisodiya S. Diaphragm myoclonus
DR. The prevalence of psychosis in epilepsy; a systematic followed by generalised atonia in a patient with trisomy 4p:
review and meta-analysis. BMC Psychiatry 2014; 14: 75. unusual semiology in an unusual condition. Epileptic Disord
2015; 17(4): 473-7.
395. Devinsky O. Postictal psychosis: common, dangerous
and treatable. Epilepsy Curr 2008; 8(2): 31-4. 412. Casaubon L, Pohlmann-Eden B, Khosravani H, Carlen
PL, Wennberg R. Video-EEG evidence of lateralized clinical
396. Kanner AM, Soto A, Gross-Kanner H. Prevalence and features in primary generalized epilepsy with tonic-clonic
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
clinical characteristics of postictal psychiatric symptoms in seizures. Epileptic Disord 2003; 5(3): 149-56.
partial epilepsy. Neurology 2004; 62(5): 708-13.
413. Jayakumar H, Gopinath S, Pillai A, Kumar A. Epileptic
397. Eisenschenk S, Krop H, Devinsky O. Homicide during nystagmus due to a large parieto-temporo-occipital multi-
postictal psychosis. Epilepsy Behav Case Rep 2014; 2: 118-20. lobar dysplasia. Epileptic Disord 2020; 22(5): 691-2.
398. Kanner AM, Trimble M, Schmitz B. Postictal affective 414. Saltik S, Cokar O, Uslu T, Uludüz D, Dervent A.
episodes. Epilepsy Behav 2010; 19(2): 156-8. Alternating hemiplegia of childhood: presentation of two
399. Barba C, Barbati G, Minotti L, Hoffmann D, Kahane P. cases regarding the extent of variability. Epileptic Disord
Ictal clinical and scalp-EEG findings differentiating temporal 2004; 6(1): 45-8.
lobe epilepsies from temporal ’plus’ epilepsies. Brain 2007; 415. Caraballo RH, Fejerman N, Bernardina BD, Ruggieri V,
130(Pt 7): 1957-67. Cersósimo R, Medina C, et al. Epileptic spasms in clusters
400. McGonigal A, Bartolomei F, Chauvel P. On seizure without hypsarrhythmia in infancy. Epileptic Disord 2003; 5
semiology. Epilepsia 2021; 62(9): 2019-35. (2): 109-13.
401. Chauvel P. Contributions of Jean Talairach and Jean 416. Umeoka S, Baba K, Terada K, Matsuda K, Tottori T, Usui
Bancaud to epilepsy surgery. Epilepsy surgery. Philadelphia: N, et al. Bilateral symmetric tonic posturing suggesting
Lippincott Williams & Wilkins, 2001. propagation to the supplementary motor area in a patient
with precuneate cortical dysplasia. Epileptic Disord 2007; 9
402. Stefan H. The challenge epilepsy treatment – New (4): 443-8.
epileptic drugs. Oxford: Blackwell science, 1998.
417. Fernández-Torre JL, Riancho J, Martín-García M, Martí-
403. Stoyke C, Bilgin O, Noachtar S. Video atlas of nez-de Las Cuevas G, Bosque-Varela P. Tonic status
lateralising and localising seizure phenomena. Epileptic epilepticus in a centenarian woman. Epileptic Disord 2019;
Disord 2011; 13(2): 113-24. 21(1): 92-6.
404. Donadío M, Ugarnes G, Segalovich M, Arakaki N, 418. Takeda T, Osawa M, Toi S, Mizuno S, Shimizu Y,
Sanchez Gonzalez F, Petre C, et al. Intracranial video-EEG Uchiyama S. Adversive seizures associated with periodic
and surgery for focal atonic seizures. Epileptic Disord 2013; lateralised epileptiform discharges (PLEDs) after left orbital
15(1): 62-6. contusion. Epileptic Disord 2012; 14(4): 422-5.
405. Hahn A, Fischenbeck A, Stephani U. Induction of 419. Gavvala JR, Gerard EE, Macken M, Schuele SU. Seizure
epileptic negative myoclonus by oxcarbazepine in symp- ending signs in patients with dyscognitive focal seizures.
tomatic epilepsy. Epileptic Disord 2004; 6(4): 271-4. Epileptic Disord 2015; 17(3): 255-62.
406. Saint-Martin AD, Carcangiu R, Arzimanoglou A, Massa 420. Mir A, Thani Z, Bashir S, Ayed H, Albaradie R. LGI-1
R, Thomas P, Motte J, et al. Semiology of typical and atypical antibody encephalitis in a seven-year-old girl. Epileptic
Rolandic epilepsy: a video-EEG analysis. Epileptic Disord Disord 2019; 21(6): 591-7.
2001; 3(4): 173-82.
421. López-Laso E, Mateos González ME, Camino León R,
407. Dragoumi P, Emery J, Chivers F, Brady M, Desurkar A, Jiménez González MD, Esparza Rodríguez J. Giant hypotha-
Cross JH, et al. Crossing the lines between epilepsy lamic hamartoma and dacrystic seizures. Epileptic Disord
syndromes: a myoclonic epilepsy variant with prominent 2007; 9(1): 90-3.
eyelid myoclonia and atonic components. Epileptic Disord
2018; 20(1): 35-41. 422. Dimova P, Boneva I, Todorova A, Minotti L, Kahane P.
Gelastic seizures in ring chromosome 20 syndrome: a case
408. Nasser H, Lopez-Hernandez E, Ilea A, Le Morvan N, report with video illustration. Epileptic Disord 2012; 14(2):
Bellavoine V, Delanoë C, et al. Myoclonic jerks are 181-6.
commonly associated with absence seizures in early-onset
absence epilepsy. Epileptic Disord 2017; 19(2): 137-46. 423. Arzimanoglou AA, Hirsch E, Aicardi J. Hypothalamic
hamartoma and epilepsy in children: illustrative cases
409. Ramanathan S, Wong CH, Rahman Z, Dale RC, Fulcher of possible evolutions. Epileptic Disord 2003; 5(4):
D, Bleasel AF. Myoclonic status epilepticus as a presentation 187-99.
Supplementary video 1
A patient with an atonic seizure, presenting as atonia of the neck and trunk musculature.
Key words for video research on www.epilepticdisorders.com
Supplementary video 2
An infant with a myoclonic seizure showing a sudden, very brief bilateral muscle jerk of the upper limbs. The
second movement is a reactive movement, as the spontaneous seizure jerk scares the child.
Key words for video research on www.epilepticdisorders.com
Phenomenology: myoclonic seizure, generalized
Localization: generalized
Syndrome: early myoclonic encephalopathy
Aetiology: genetic disorder
Supplementary video 3
A patient with a bilateral synchronous clonic seizure.
Key words for video research on www.epilepticdisorders.com
Phenomenology: clonic seizure
Localization: generalized
Syndrome: unknown
Aetiology: unknown
Supplementary video 4
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
A young child with a generalized seizure, starting with a bilateral muscle jerk in the shoulders (myoclonic),
followed by muscle activity cessation (atonia), resulting in a fall.
Key words for video research on www.epilepticdisorders.com
Phenomenology: myoclonic atonic seizure
Localization: generalized
Syndrome: Doose syndrome
Aetiology: idiopathic
Supplementary video 5
A focal seizure with impaired awareness arising from the frontal lobe during sleep. Note that the patient is
sleeping on a mattress on the floor with protective mattresses around him. The seizure starts with fulminant
hyperkinetic behavior, followed by a gyratory movement of the body to the right. The patient’s awareness is
impaired and he is not responding to the nurse’s commands. In the immediate postictal phase, the patient
becomes responsive, and is able to point to the window, in response to the verbal command.
Key words for video research on www.epilepticdisorders.com
Phenomenology: hypermotor seizure, gyratory (not from the existing list)
Localization: frontal prefrontal mesiolateral
Syndrome: focal, non-idiopathic frontal (FLE)
Aetiology: unknown
Supplementary video 6
An infant with clusters of epileptic spasms. Note the typical gestalt of the spasms with flexion in the neck and
simultaneous abduction in the shoulders and flexion in the hips.
Key words for video research on www.epilepticdisorders.com
Phenomenology: spasm (epileptic)
Localization: generalized
Syndrome: west syndrome
Aetiology: genetic disorder
Supplementary video 7
Generalized tonic-clonic seizure occurring during sleep. The patient lies in the bed in prone position. The
seizure starts with ictal crying -the characteristic sound produced by the forced push of air through the
airways, due to the tonic contraction of the diaphragm. Symmetric tonic contraction of all four limbs is then
observed, followed by symmetric clonic jerks which gradually decrease in frequency.
Key words for video research on www.epilepticdisorders.com
Phenomenology: generalized, tonic-clonic seizure
Localization: generalized
Syndrome: idiopathic generalized not specified
Aetiology: idiopathic/genetic predisposition
Supplementary video 8
The patient is sitting in bed and watching TV. The seizure starts abruptly with fearful behavior, followed by
integrated automatisms. During the seizure, there is impaired awareness. After the seizure ends, the patient
answers the nurse’s questions and follows commands.
Key words for video research on www.epilepticdisorders.com
Phenomenology: fear, hypermotor seizure
Localization: frontal, prefrontal mesial
Syndrome: focal non-idiopathic frontal (FLE)
Aetiology: focal cortical dysplasia
Copyright © 2022 John Libbey Eurotext. Downloaded by DR JOSE ZAPATA BERRUECOS on 21/05/2022.
Supplementary video 9
A focal impaired awareness seizure that starts with gestural automatisms and continues with ictal aphasia. The
patient does not follow verbal commands, but follows visual clues.
Key words for video research on www.epilepticdisorders.com
Phenomenology: aphasic seizure, cognitive (not in the list), automatisms
Localization: left temporal lobe
Syndrome: focal non-idiopathic mesiotemporal (MTLE with or without HS)
Aetiology: hippocampal sclerosis