Concept information
Término preferido
Pantothenate Kinase-Associated Neurodegeneration
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Tipo
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mesh:Descriptor
Definición
- 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. (From Adams et al., Principles of Neurology, 6th ed, p972; Davis & Robertson, Textbook of Neuropathology, 2nd ed, pp972-929)
Concepto genérico
Etiquetas alternativas
- Hallervorden-Spatz Disease
- Hallervorden-Spatz Syndrome
- Neuroaxonal Dystrophy, Juvenile-Onset
- Neurodegeneration With Brain Iron Accumulation 1
- Neurodegeneration with Brain Iron Accumulation Type 1
- Pigmentary Pallidal Atrophy
- Pigmentary Pallidal Degeneration
- PKAN Neuroaxonal Dystrophy, Juvenile-Onset
En otras lenguas
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francés
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Dégénérescence pallidale pigmentaire
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Dystrophie neuro-axonale tardive
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Dystrophie neuroaxonale tardive
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Maladie de Hallervorden-Spatz
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Neurodégénerescence avec accumulation de fer dans le cerveau
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Neuroferritinopathie
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Syndrome de Hallervorden-Spatz
URI
http://data.loterre.fr/ark:/67375/JVR-VNH65KKH-P
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