How broad is the phenotype of Hallervorden-Spatz disease?

Hickman, S J; Ward, N S; Surtees, R A; Stevens, J M; Farmer, S F

Hickman, S J; Ward, N S; Surtees, R A; Stevens, J M; Farmer, S F.

Affiliation

Hickman SJ; Department of Neurology, The National Hospital for Neurology and Neurosurgery, London, UK. s.hickman@ion.ucl.ac.uk

Acta Neurol Scand ; 103(3): 201-3, 2001 Mar.

Article in En | MEDLINE | ID: mdl-11240570

Subject(s)

Cognition Disorders/etiology; Motor Skills Disorders/etiology; Pantothenate Kinase-Associated Neurodegeneration/pathology; Adult; Age of Onset; Dystonia/etiology; Female; Globus Pallidus/pathology; Humans; Iron/analysis; Magnetic Resonance Imaging; Phenotype; Substantia Nigra/pathology

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Collection: 01-internacional Database: MEDLINE Main subject: Cognition Disorders / Motor Skills Disorders / Pantothenate Kinase-Associated Neurodegeneration Type of study: Etiology_studies Limits: Adult / Female / Humans Language: En Journal: Acta Neurol Scand Year: 2001 Document type: Article Affiliation country: United kingdom Country of publication: Denmark

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