MeSH 搜索器

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)
副标题
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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