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Taylor TD, Litt M, Kramer P, et al. Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13. Nat Genet. Dec 1996;14(4):479-81. [Medline].
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Pantothenate kinase-associated neurodegeneration - Wikipedia, the free encyclopedia
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Hallervorden-Spatz syndrome: A very rare disease with degeneration of the globus pallidus, red nucleus, and substantia nigra of the brain. It is characterized by progressive Parkinson-like rigidity, athetotic movements, and progressive mental and emotional retardation. ... A heredo-familial syndrome, ... Hallervorden-Spatz disease;
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MIM #234200 · Text · Description · Clinical Features · Diagnosis · Mapping · Molecular Genetics · Genotype/Phenotype Correlations · Population Genetics ...
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Definition of Hallervorden-Spatz syndrome in the Medical Dictionary. Hallervorden-Spatz syndrome explanation. Information about Hallervorden-Spatz syndrome in Free online English dictionary. What is Hallervorden-Spatz syndrome? ... Hallervorden-Spatz syndrome; hallex; Hallion's test; Hallopeau's disease;
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NORD: Neurodegeneration with Brain Iron Accumulation Type 1 - Offers synonyms, a general discussion and further resources for the disorder formerly known as Hallervorden-Spatz Syndrome.
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Links to information and resources for Hallervorden-Spatz syndrome, an inherited neurological movement disorder. ... OHSU: Hallervorden-Spatz Syndrome; Good overview of the Hallervorden-Spatz disorders and Oregon Health Science University research, by Susan J. Hayflick, MD...
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En Español | Plain Text Version | Skip Navigation ... National Institutes of Health ... Synonym(s): Hallervorden-Spatz Disease, Pantothenate Kinase-Associated Neurodegeneration;
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The First Scientific Workshop of Hallervorden-Spatz Syndrome; Grant Number: NS40452-01; May 19 - 20, 2000; National Institute of Neurological Disorders & Stroke, Bethesda, Maryland; Principal Investigator: Susan J. Hayflick, MD;
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