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Case Report
Sturge Weber Syndrome with Bilateral Port-Wine Nevus
Author(s): Chitlangia M, Parakh P, Yadav S, Shah GS and Mishra OPChitlangia 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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DOI:
10.4172/2165-7920.1000180
Journal of Clinical Case Reports received 1345 citations as per Google Scholar report