Journal of Clinical Case Reports

Sturge Weber Syndrome with Bilateral Port-Wine Nevus

Abstract

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.