EAS Publisher | Sturge-Weber Syndrome: About A Case

Sturge-Weber Syndrome: About A Case

DOI : https://doi.org/10.36349/easjrit.2022.v04i04.008

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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.

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Lecturer, Dept. of Pharmacology and Therapeutics, Shaheed Monsur Ali Medical College & Hospital, Uttara, Dhaka-1230, Bangladesh

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