[The Hallervorden-Spatz Disease].
D000293:Adolescent; D000328:Adult; D000368:Aged; D001369:Axons; D001927:Brain Diseases / Q000235:genetics / Q000473:pathology*; D002525:Cerebellar Cortex / Q000473:pathology; D002531:Cerebellum / Q000473:pathology; D002540:Cerebral Cortex / Q000473:pathology*; D002648:Child; D005260:Female; D005917:Globus Pallidus / Q000473:pathology*; D006801:Humans; D008297:Male; D008526:Medulla Oblongata / Q000473:pathology; D009069:Movement Disorders / Q000473:pathology*; D009410:Nerve Degeneration; D006211:Pantothenate Kinase-Associated Neurodegeneration / Q000473:pathology; D013116:Spinal Cord / Q000473:pathology; D013378:Substantia Nigra / Q000473:pathology*; D013788:Thalamus / Q000473:pathology; D014811:Vitamin E Deficiency
Die Hallervorden-Spatzsche Krankheit.