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Sturge-Weber Syndrome
Hierarchy: | ∟ ∟ ∟ Sturge-Weber Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | ∟ ∟ ∟ Sturge-Weber Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome ∟ ∟ ∟ Sturge-Weber Syndrome ∟ ∟ ∟ ∟ Sturge-Weber Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Sturge-Weber Syndrome ∟ ∟ ∟ ∟ Sturge-Weber Syndrome |
historyNote*: | 91(75); was see under ANGIOMATOSIS 1975-90; DIMITRI DISEASE was see STURGE-WEBER SYNDROME 1989-93
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onlineNote*: | search ANGIOMATOSIS 1966-74; use STURGE-WEBER SYNDROME to search DIMITRI DISEASE 1989-93
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publicMeSHNote*: | 91; was see under ANGIOMATOSIS 1975-90; DIMITRI DISEASE was see STURGE-WEBER SYNDROME 1989-93
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Scope note: | A congenital syndrome characterized by a port-wine nevus covering portions of the face and cranium (in the distribution of the ophthalmic division of the TRIGEMINAL NERVE) and angiomas of the meninges and choroid. Clinical manifestations include the onset of focal SEIZURES, progressive hemiparesis, GLAUCOMA, hemianopsia, and cognitive deficits in the first decade of life. By age two years, skull radiographs reveal "tramline calcifications" of the margins of the occipital and parietal lobes. Pathologically cortical neurons are replaced by glial tissue that undergoes calcification. (From Adams et al., Principles of Neurology, 6th ed, pp1018-9)
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Sturge-Weberin oireyhtymä (fi) XSturge-Weberin syndrooma (fi, replaced) Sturge-Webers syndrom (sv) Sturge-Weber-Dimitri Syndrome (en, replaced) Sturge-Kalischer-Weber Syndrome (en, replaced) Sturge-Weber-Krabbe Syndrome (en, replaced) Sturge's Syndrome (en, replaced) Sturge Syndrome (en, replaced) Sturge Disease (en, replaced) Meningo-Oculo-Facial Angiomatosis (en, replaced) Encephalofacial Hemangiomatosis Syndrome (en, replaced) Meningofacial Angiomatosis-Cerebral Calcification Syndrome (en, replaced) Neuroretinoangiomatosis (en, replaced) Phakomatosis, Sturge-Weber (en, replaced) Angiomatosis Oculoorbital-Thalamic Syndrome (en, replaced) Syndroma Sturge-Weber (la-FI, replaced) |
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