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- W2332491612 abstract "Sturge-Weber syndrome, sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder. It is one of the phakomatoses and is often associated with port-wine stains of the face, glaucoma, seizures, mental retardation, and ipsilateral leptomeningeal angioma (cerebral malformations and tumors). It is characterized by abnormal blood vessels on the brain surface. Normally, only one side of the brain is affected. We report a case of 13 year old female child with facial port wine stains along with radiological features which showed tram track sign and cortical atrophy in the right parietal lobe." @default.
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- W2332491612 date "2014-09-22" @default.
- W2332491612 modified "2023-09-24" @default.
- W2332491612 title "STURGE WEBER SYNDROME: A CASE REPORT WITH CLINICAL AND RADIOLOGICAL FEATURES" @default.
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- W2332491612 doi "https://doi.org/10.14260/jemds/2014/3476" @default.
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