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Sturge-Weber Syndrome  

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Tipo

  • mesh:Descriptor

Definición

  • 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.

Etiquetas alternativas

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

En otras lenguas

  • francés

  • Angiomatose congénitale de Sturge-Weber-Krabbe
  • Angiomatose encéphalo-trigéminée
  • Angiomatose encéphalotrigéminée
  • Maladie de Sturge-Weber-Krabbe
  • Neuro-angiomatose encéphalo-faciale
  • Neuroangiomatose encéphalofaciale
  • Phacomatose de Sturge-Weber-Krabbe
  • SWK (Syndrome de Sturge-Weber-Krabbe)
  • Syndrome de Sturge-Weber-Krabbe

URI

http://data.loterre.fr/ark:/67375/JVR-ZCL90G3X-N

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