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