Sturge Weber Syndrome Diagnosed at Late Age, Associated with Psychiatric Complaints and Status: A Case Report

Sturge-Weber syndrome (SWS) is a rare, sporadic neurocutaneous syndrome characterized by a usually unilateral facial port-wine stain, ipsilateral leptomeningeal angiomatosis, glaucoma, epileptic seizures that are difficult to control, and progressive cerebral dysfunction. A 41-year-old woman present...

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Bibliographic Details
Main Authors: Hilal TAŞTEKİN TOZ, Eren GÖZKE, Boran Can SARAÇOĞLU
Format: Article
Language:English
Published: Galenos Yayinevi 2018-08-01
Series:Archives of Epilepsy
Subjects:
Online Access: http://archepilepsy.org/archives/archive-detail/article-preview/sturge-weber-syndrome-diagnosed-at-late-age-associ/54903