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Diagnostic dilemma: Sturge-Weber syndrome, without facial nevus

Sturge-Weber syndrome (SWS), a rare sporadic neurocutaneous disease, is characterized by a congenital unilateral port-wine nevus affecting the area innervated by V1, ipsilateral leptomeningeal angiomatosis, and calcification in the occipital or frontoparietal region and glaucoma/vascular eye abnorma...

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Detalles Bibliográficos
Autores principales:	Zanzmera, Paresh, Patel, Tinkal, Shah, Vinay
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2015
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4244768/ https://www.ncbi.nlm.nih.gov/pubmed/25552865 http://dx.doi.org/10.4103/0976-3147.143215

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