Category:Sturge–Weber syndrome

**Sturge–Weber syndrome**
	neurological and skin disorder associated with port-wine stains of the face, glaucoma, seizures, intellectual disability, and cerebral malformations
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Instance of	rare disease; head and neck disease; developmental defect during embryogenesis; designated intractable/rare disease; class of disease;
Subclass of	phakomatosis; overgrowth syndrome; cerebral diseases of vascular origin with epilepsy; neurocutaneous syndrome with epilepsy; syndrome or malformation associated with head and neck malformations; skull cancer; brain cancer; rare capillary malformation with associated anomalies; palpebral tumor with a vascular malformation; rare genetic vascular tumor; conjunctival cancer; conjunctival hemangioma or hemolymphangioma; syndromic glaucoma; central nervous system vascular malformation; syndromic developmental defect of the eye; vascular disease; disease;
Named after	William Allen Sturge; Frederick Parkes Weber;
Authority file
	Q1886238; BabelNet ID: 01888122n
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Radiology: Computed tomography · Magnetic resonance |

<nowiki>Síndrome de Sturge-Weber; syndrome de Sturge-Weber; Энцефалотригеминальный ангиоматоз; Sturge-Weber-Syndrom; Síndrome de Sturge-Weber; سندروم استرج-وبر; 斯特奇-韦伯综合征; Sturge-Weber sendromu; スタージー・ウェーバー症候群; กลุ่มอาการสเตอร์จ-เวเบอร์; Zespół Sturge'a-Webera; sturge-weber syndrom; Syndroom van Sturge-Weber; 斯特奇-韋伯綜合征; 斯特奇-韦伯综合征; Sindrome di Sturge-Weber; 斯特奇-韋伯綜合征; Sturge–Weber syndrome; متلازمة ستيرج ويبر; Стерџ-Веберов синдром; Стердж-Вебер синдромы; neurological and skin disorder associated with port-wine stains of the face, glaucoma, seizures, intellectual disability, and cerebral malformations; angeborene fortschreitende Erkrankung aus der Gruppe der neurokutanen Phakomatosen; Sindrome de Sturger Weber; Síndrome de Sturger Weber; Síndrome de Sturge Weber; Sindrome Sturger Weber; Sindrome Stuger Weber; Enfermedad de Dimitri; Sindrome Stuger-Weber; Angiomatosis meningea capilar; Sindrome de Sturge Weber; Angiomatosis encefalofacial; Síndrome de Stuger Weber; Angiomatosis meníngea capilar; Sindrome de Sturge-Weber; Sindrome de Stuger Weber; スタージ・ウェバー症候群; Syndrome de Sturge-Weber-Krabbe; Choroba Sturge'a-Webera; Naczyniakowatość twarzowo-mózgowa; Choroba Sturge'a i Webera; Zespół Sturge'a i Webera; Ziekte van Sturge-Weber; Болезнь Штурге-Вебера; Синдром Штурге-Вебера; Ангиоматоз энцефалотригеминальный; Sturge-Weber-Krabbe-Syndrom; Angiomatosis encephalofacialis; encephalotrigeminal angiomatosis; Sturge-Weber-Krabbe disease; Sturge-Weber syndrome; Sturge-Weber Syndrome; Sturge-Weber-Krabbe syndrome; SWS type II - Facial angioma alone, no CNS involvement; SWS type III - Isolated leptomeningeal angiomas; Sturge-Weber-Krabbe angiomatosis; Sturge-Weber Disease; Meningeal capillary angiomatosis; Leptomeningeal angiomatosis; Encephalofacial angiomatosis; Sturge-Weber-Dimitri syndrome; Sturge Weber syndrome; STURGE-WEBER SYNDROME; SWS; SWS; Encephalotrigeminal Syndrome; SWS type I - Facial and leptomeningeal angiomas; Fourth phacomatosis; 斯特奇–韦伯综合征; Sindrome di Parkes Weber-Dimitri; Sindrome di Sturge Weber; Angiomatosi encefalo-facciale; Angiomatosi meningofacciale; Angiomatosi encefalotrigeminale; Angiomatosi encefalo-trigeminale</nowiki>