Sturge–Weber syndrome in a 6-year-old girl
Sturge–Weber syndrome (SWS), or encephalotrigeminal angiomatosis, is a rare, non-hereditary condition characterized by a facial cutaneous vascular nevus (nevus flammeus or port wine stain) in association with leptomeningeal angiomatosis [1,2].
| Main Author: | D. E. C. PEREZ, J. S. PEREIRA NETO, E. GRANER, & M. A. LOPES |
|---|---|
| Format: | Koleksi Audio Visual |
| Language: | Bahasa Inggris |
| Published: |
Paediatric Dentistry
2005
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| Subjects: | |
| Online Access: |
http://oaipmh-jogjalib.umy.ac.idkatalog.php?opo=lihatDetilKatalog&id=94309 |