Sturge-Weber Syndrome: About A Case

Abstract

Sturge-Weber syndrome (SWS) or encephalo-facial angiomatosis, is a syndrome rare congenital neurocutaneous and ocular. He has two types of malformations: capillary congenital facial with flat angioma type and capillaro-venous lepto-meningeal location the more often ipsilateral parieto-occipital. The Neuroimaging, essentially imaging by magnetic resonance (MRI), plays a role important in establishing the diagnosis, ideally before the onset of complications neuro-ocular. We report the case of a patient with motor impairment in whom SWS is suspected based on facial angioma and pharmaco-resistant epilepsy.