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A Case of Spinocerebellar Ataxia Type 6 with Hypochondriasis and Severe Parkinsonism Ichiro Kohira 1 , Hiroshi Ujike 2 , Takeshi Katsu 3 , Yotaro Ninomiya 1 , Kazuyo Ohashi 1 1Department of Neurology, Kochi Municipal Central Hospital 2Department of Neuropsychiatry, Okayama University Medical School 3Geshi Hospital Keyword: spinocerebellar ataxia type 6 , parkinsonism , genomic testing , sporadic spinocerebellar degeneration , negative family history pp.1119-1122
Published Date 2001/12/1
DOI https://doi.org/10.11477/mf.1406901876
  • Abstract
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We report a case of 68-year-old woman who wasdiagnosed spinocerebellar ataxia type 6 (SCA 6) by genomic testing. She presented hypochondriasis , parkinsonism, and ataxia. Since the age of 60, she noted difficulty in walking due to dizziness, and MRI showed minimal cerebellar atrophy. She became un-able to walk without assistance at the age 67. She was referred to us when she was 68 years old. She had no family history of cerebellar ataxia, and her general physical examination was normal.


Copyright © 2001, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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