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Hallervorden-Spatz Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ Hallervorden-Spatz Syndrome 38 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hallervorden-Spatz Syndrome 38 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hallervorden-Spatz Syndrome 38 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hallervorden-Spatz Syndrome 38 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hallervorden-Spatz Syndrome 38 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | ∟ ∟ ∟ ∟ Hallervorden-Spatz Syndrome ∟ ∟ ∟ ∟ ∟ Hallervorden-Spatz Syndrome ∟ ∟ ∟ ∟ ∟ Hallervorden-Spatz Syndrome ∟ ∟ ∟ ∟ Hallervorden-Spatz Syndrome ∟ ∟ ∟ ∟ Hallervorden-Spatz Syndrome |
Annotation: | DF: HALLERVORDEN SPATZ DIS
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historyNote*: | 1991(1965)
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publicMeSHNote*: | 1991; see BASAL GANGLIA DISEASES 1979-1990, see BRAIN DISEASES 1975-78
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Scope note: | A rare autosomal recessive degenerative disorder which usually presents in late childhood or adolescence. Clinical manifestations include progressive MUSCLE SPASTICITY; hyperreflexia; MUSCLE RIGIDITY; DYSTONIA; DYSARTHRIA; and intellectual deterioration which progresses to severe dementia over several years. Pathologic examination reveals neuronal atrophy in the globus pallidus and iron deposition in blood vessels and perivascular spaces. (From Adams et al., Principles of Neurology, 6th ed, p972; Davis & Robertson, Textbook of Neuropathology, 2nd ed, pp972-929)
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | NLMX |
Type: | |
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Labels and equivalent concepts: | Pigmentoitunut pallidusrappeuma (fi) XHallervorden-Spatzin tauti (fi, replaced) Hallervorden-Spatzin syndrooma (fi, replaced) Hallervorden-Spatzin oireyhtymä (fi, replaced) Hallervorden-Spatzs syndrom (sv) Pigmentary Pallidal Atrophy (en, replaced) Pigmentary Pallidal Degeneration (en, replaced) Hallervorden-Spatz Disease (en, replaced) Degeneratio globi pallidi pigmentata (la-FI, replaced) Morbus Hallervorden-Spatz (la-FI, replaced) Syndroma Hallervorden-Spatz (la-FI, replaced) |
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