Journal of Clinical Case Reports

ISSN: 2165-7920

Open Access

Sturge Weber Syndrome with Bilateral Port-Wine Nevus


Chitlangia M, Parakh P, Yadav S, Shah GS and Mishra OP

Sturge-Weber syndrome is a rare neurocutaneous syndrome characterized by port -wine stain, seizures and intracranial calcifications.The present case had bilateral port-wine nevus, generalised tonic-clonic seizures and right sided intracranial calcifications involving right temporo-parieto-occipital lobe regions with prominent choroid plexus.


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