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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Sturge Weber Syndrome — Syndrome, Sturge-Weber — Sturge Disease — Sturge Syndrome — Syndrome, Sturge — Sturge's Syndrome — Syndrome, Sturge's — Sturge-Kalischer-Weber Syndrome — Sturge Kalischer Weber Syndrome — Syndrome, Sturge-Kalischer-Weber — Neuroretinoangiomatosis — Sturge-Weber-Krabbe Syndrome — Sturge Weber Krabbe Syndrome — Syndrome, Sturge-Weber-Krabbe — Angiomatosis Oculoorbital-Thalamic Syndrome — Encephalofacial Hemangiomatosis Syndrome — Hemangiomatosis Syndrome, Encephalofacial — Syndrome, Encephalofacial Hemangiomatosis — Meningo-Oculo-Facial Angiomatosis — Angiomatosis, Meningo-Oculo-Facial — Meningo Oculo Facial Angiomatosis — Meningofacial Angiomatosis-Cerebral Calcification Syndrome — Phakomatosis, Sturge-Weber — Phakomatosis, Sturge Weber — Sturge-Weber Phakomatosis — Sturge-Weber-Dimitri Syndrome — Sturge Weber Dimitri Syndrome — Syndrome, Sturge-Weber-Dimitri — Parkes Weber Syndrome — Syndrome, Parkes Weber — Parkes-Weber Syndrome — Syndrome, Parkes-Weber