Sturge-Weber Syndrome
ABSTRACT The Sturge-Weber Syndrome (SWS) is rare, congenital and nonhereditary neurocutaneous affection, characterized by leptomeningeal and cutaneous angiomas. We report a case of a child with symptomatology and radiology compatible with SWS, however without facial nevus.
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Format: | Article |
Language: | Portuguese |
Published: |
Pontifícia Universidade Católica de São Paulo
2013-09-01
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Series: | Revista da Faculdade de Ciências Médicas de Sorocaba |
Subjects: | |
Online Access: | http://revistas.pucsp.br/index.php/RFCMS/article/view/8900 |