Sturge Weber Syndrome: A Case Report.
Article
in English
| IMSEAR
| ID: sea-147087
ABSTRACT
Sturge-Weber syndrome is a neurocutaneous syndrome characterized by port wine stain, congenital glaucoma, and underlying anomalous leptomeningeal venous plexus and the lack of normal cortical venous drainage. It is a congenital but not an inherited disease and it occurs sporadically and is very rare, incidence being approximately 1 on 50000. It occurs with rare exception but occasionally the other members of the family may have hemangiomata of a lesser degree.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Language:
English
Year:
2010
Type:
Article
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