Concept information
Término preferido
Sturge-Weber Syndrome
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Tipo
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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.
Concepto genérico
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
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francés
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Angiomatose congénitale de Sturge-Weber-Krabbe
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Angiomatose encéphalo-trigéminée
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Angiomatose encéphalotrigéminée
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Maladie de Sturge-Weber-Krabbe
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Neuro-angiomatose encéphalo-faciale
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Neuroangiomatose encéphalofaciale
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Phacomatose de Sturge-Weber-Krabbe
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SWK (Syndrome de Sturge-Weber-Krabbe)
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Syndrome de Sturge-Weber-Krabbe
URI
http://data.loterre.fr/ark:/67375/JVR-ZCL90G3X-N
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