Sturge–Weber syndrome in a 6-year-old girl
Author
: D. E. C. PEREZ, J. S. PEREIRA NETO, E. GRANER, & M. A. LOPES
Publisher
: Paediatric Dentistry
Summary :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].
Copies :
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08195158 |
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