Topic 7 Cell Division.pdf
Topic 7 Cell Division.pdf
Topic 7 Cell Division.pdf
Gametes have half the number of chromosomes that body cells have.
Autosomal Trisomy
Trisomy 13 (Patau Syndrome) a genetic disorder in which a person has 3 copies
of genetic material from chromosome 13, instead of the usual 2 copies. Rarely,
the extra material may be attached to another chromosome.
Trisomy 18 (Edward Syndrome) -disorder in which babies are born with 3 copies
of chromosome 18 instead of 2. For an unknown reason, this accident occurs at
the time of conception and all cells in the body will have this structure.
Trisomy 21 (Down Syndrome)- Babies with Down syndrome however, end up
with three chromosomes at position 21, instead of the usual pair.
Sex cells Trisomy
• Klinefelter Syndrome- (sometimes called Klinefelter's, KS or XXY) is where boys
and men are born with an extra X chromosome.
• Turner Syndrome -a condition that affects only females, results when one of the
X chromosomes (sex chromosomes) is missing or partially missing
Klinefelter Syndrome
Physical characteristics
Many people with triple X are taller than their peers. They’re also
often taller than pediatricians predicted based on their parents’
heights. Other, more subtle physical attributes include:
- Wide-spaced eyes (hypertelorism).
- Vertical skin folds that cover the inner corners of the eyes
(epicanthal folds).
- Curved or bent little fingers (clinodactyly).
- Poor muscle tone (hypotonia).
Neurological conditions
-Some people with triple X syndrome have developmental delays or mental health
conditions. These may include:
Developmental delays.
Learning disabilities.
Attention-deficit/hyperactivity disorder.
Mood disorders like anxiety and depression.
Mild cognitive impairment.
KEY CONCEPT
During meiosis, diploid cells undergo two cell divisions that result in haploid cells.
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OOGENESIS SPERMATOGENESIS