Sturge –Weber Syndrome – A Case Report
Journal Title: Journal of Medical Science And clinical Research - Year 2017, Vol 5, Issue 7
Abstract
Sturge-Weber Syndrome or encephalotrigeminal angiomatosis is a rare congenital, non-familial disorder characterized by a congenital facial birthmark and neurological abnormalities. The GNAQ gene mutation is responsible for Sturge-Weber syndrome.
Authors and Affiliations
Dr Selvakumar Subbaraman
Keywords
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