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.
Partagez cet article
English 
Spanish 
Chinese 
Russian 
German 
Japanese 
Portuguese 
Hindi 