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.
推出的年份: 1991(1975)
树号: C04.557.645.375.850, C10.562.800, C14.907.077.850
MeSH 单一 ID: D013341
进入的组:
Sturge Weber Syndrome
Syndrome, Sturge-Weber
Parkes Weber Syndrome
Syndrome, Parkes 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
Sturge-Weber-Dimitri Syndrome
Sturge Weber Dimitri Syndrome
Syndrome, Sturge-Weber-Dimitri
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
Neuroretinoangiomatosis
Parkes-Weber Syndrome
Syndrome, Parkes-Weber
Phakomatosis, Sturge-Weber
Phakomatosis, Sturge Weber
Sturge-Weber Phakomatosis
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