Other terms
Sturge Weber Syndrome,Syndrome, Sturge-Weber,Sturge's Syndrome,Syndrome, Sturge's,Sturge-Kalischer-Weber Syndrome,Sturge Kalischer Weber Syndrome,Syndrome, Sturge-Kalischer-Weber,Sturge-Weber-Dimitri Syndrome,Sturge Weber Dimitri Syndrome,Syndrome, Sturge-Weber-Dimitri,Neuroretinoangiomatosis,Neuroretinoangiomatoses,Encephalofacial Hemangiomatosis Syndrome,Encephalofacial Hemangiomatosis Syndromes,Hemangiomatosis Syndrome, Encephalofacial,Hemangiomatosis Syndromes, Encephalofacial,Syndrome, Encephalofacial Hemangiomatosis,Syndromes, Encephalofacial Hemangiomatosis,Angiomatosis Oculoorbital-Thalamic Syndrome,Meningo-Oculo-Facial Angiomatosis,Angiomatoses, Meningo-Oculo-Facial,Angiomatosis, Meningo-Oculo-Facial,Meningo Oculo Facial Angiomatosis,Meningo-Oculo-Facial Angiomatoses,Meningofacial Angiomatosis-Cerebral Calcification Syndrome,Meningofacial Angiomatosis Cerebral Calcification Syndrome,Sturge Disease,Sturge-Weber-Krabbe Syndrome,Sturge Weber Krabbe Syndrome,Syndrome, Sturge-Weber-Krabbe,Sturge Syndrome,Syndrome, Sturge,Phakomatosis, Sturge-Weber,Phakomatosis, Sturge Weber,Sturge-Weber Phakomatosis
Description
Sturge-Weber Syndrome: A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects.
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