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Синдром Стурджа-Вебера

ORPHA:3205· ICD-10 Q85.8· Sturge-Weber syndrome

Визначення(English summary)

A rare congenital neurocutaneous syndrome defined by a facial capillary malformation or port-wine birthmark (PWB) associated with cerebral and ocular ipsilateral vascular malformations in most of the cases resulting in variable ocular and neurological complications.

Поширеність
1-9 / 100 000
Успадкування
Not applicable
Вік початку
Antenatal, Neonatal