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DeCS
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Descriptor English:
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Sturge-Weber Syndrome
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Descriptor Spanish:
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Síndrome de Sturge-Weber
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Descriptor Portuguese:
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Síndrome de Sturge-Weber
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Synonyms English:
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Neuroretinoangiomatosis
Phakomatosis, Sturge-Weber
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Tree Number:
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C04.557.645.375.850
C10.562.800
C14.907.077.850
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Definition English:
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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. |
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History Note English:
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91(75); was see under ANGIOMATOSIS 1975-90; DIMITRI DISEASE was see STURGE-WEBER SYNDROME 1989-93
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Allowable Qualifiers English:
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Record Number:
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24333
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Unique Identifier:
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D013341
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Occurrence in VHL:
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Similar:
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DeCS CID-10 SciELO LILACS LIS
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