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- W1724494332 abstract "Sturge–Weber syndrome (encephalofacial angiomatosis) is characterized by a venous malformation involving the skin, brain, and sometimes the eye. Most patients with brain involvement develop epileptic seizures, and many of these individuals are also cognitively impaired. Some patients develop focal neurological deficits such as hemiparesis, hemiatrophy, and visual field defects. Glaucoma is common. The syndrome is sporadic and occurs in all ethnic groups (Bodensteiner & Roach, 1999)." @default.
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- W1724494332 date "2004-01-08" @default.
- W1724494332 modified "2023-10-17" @default.
- W1724494332 title "Sturge–Weber syndrome" @default.
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- W1724494332 doi "https://doi.org/10.1017/cbo9780511545054.025" @default.
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