A case of spinocerebellar ataxia type 6 with hypochondriasis and severe parkinsonism

Brain and Nerve

Volumn 53, Issue 12, 2001, Pages 1119-1122

  Kohira, Ichiro ^a   Ujike, Hiroshi ^a   Katsu, Takeshi ^a   Ninomiya, Yotaro ^a   Ohashi, Kazuyo ^a  

^a Kochi Municipal Central Hospital   (Japan)

Author keywords

Genomic testing; Negative family history; Parkinsonism; Spinocerebellar ataxia type 6; Sporadic spinocerebellar degeneration

Indexed keywords

LEVODOPA;

AGED; AKINESIA; ARTICLE; CASE REPORT; CLINICAL FEATURE; DEGENERATIVE DISEASE; DIFFERENTIAL DIAGNOSIS; DISEASE SEVERITY; FAMILY HISTORY; FEMALE; GAIT; GENETIC ANALYSIS; HUMAN; HYPOCHONDRIASIS; NEUROLOGIC EXAMINATION; PARKINSONISM; PHYSICAL EXAMINATION; SPINOCEREBELLAR DEGENERATION; TENDON REFLEX;

AGED; BRAIN; CALCIUM CHANNELS; FEMALE; HUMANS; HYPOCHONDRIASIS; MAGNETIC RESONANCE IMAGING; PARKINSON DISEASE; SPINOCEREBELLAR ATAXIAS;

EID: 0035700263     PISSN: 00068969     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Diffusion-and T 2-weighted MRI of transverse pontine fibers in spinocerebellar degeneration
2. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinico-pathological study of 100 cases
3. Spinocerebellar type 6: Molecular and clinical features of 35 Japanese patients including one homozygous for the CAG repeat expansion
4. Spinocerebellar ataxia type 6: Genotype and phenotype in German kindreds
5. Extrapyramidal motor signs in degenerative ataxias