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  1. Public
  2. 研究紀要
  3. ACTA MEDICA KINDAI UNIVERSITY
  4. 17(2)1992

A case of chronic and progressive choreiform movemetnt disorder with evident familial History

https://kindai.repo.nii.ac.jp/records/2003348
https://kindai.repo.nii.ac.jp/records/2003348
9f677671-3d0e-4a3e-b77e-89b584e6ce62
名前 / ファイル ライセンス アクション
AA0050842X-19921100-0183.pdf AA0050842X-19921100-0183.pdf (682.9 KB)
アイテムタイプ 紀要論文 / departmental bulletin paper(1)
公開日 2025-08-06
タイトル
タイトル A case of chronic and progressive choreiform movemetnt disorder with evident familial History
言語 en
作成者 Hashimoto, Atsutaka

× Hashimoto, Atsutaka

en Hashimoto, Atsutaka
Kinki University

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Nakamura, Kimi

× Nakamura, Kimi

en Nakamura, Kimi
Kinki University

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Yanai, Mika

× Yanai, Mika

en Yanai, Mika
Kinki University

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Tsuruta, Chihiro

× Tsuruta, Chihiro

en Tsuruta, Chihiro
Kinki University

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Iida, Masashi

× Iida, Masashi

en Iida, Masashi
Kinki University

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Hanada, Masanori

× Hanada, Masanori

en Hanada, Masanori
Kinki University

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言語
言語 eng
キーワード
主題 chorea, family history, dentatoruburopallidoluysian atrophy, caudate nucleus, cerebral white matter
内容記述
内容記述タイプ Abstract
内容記述 A case of chronic and progressive choreiform movement disorder with evident familial history was reported. The patient, a 68-year-old housewife, developed typical involuntary movement and psychotic symptoms concomitant with Huntington's chroea. Familial history genetically indicates autosomal dominant penetrance. Her elder sister was diagnosed with Huntington's chorea at a local public hospital. Her son was diagnosed with chronic schizophrenia and has been treated medically. Choreiform movement, however, was not indicated in the son. Thus familial history of movement disorder is significant. However, certain factors made the diagnosis of Huntington's chorea questionable in this case. Atrophy of the caduate nucleus was not evident in plain brain CT films, although hypodensity of the cerebral whitematter was not negligible. Cerebellar signs such as dysmetria or ataxic gait were prominent though in the later stage. These results strongly suggest that this was a case of pseudo-Huntington form (Hirayama) of dentatoruburopallidoluysian atrophy rather than Huntington's chorea.
言語 en
出版者
出版者 The Kinki University Medical Association
言語 en
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ departmental bulletin paper
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
収録物識別子
収録物識別子タイプ PISSN
収録物識別子 03866092
開始ページ
開始ページ 183
終了ページ
終了ページ 190
書誌情報 en : ACTA MEDICA KINKI UNIVERSITY

巻 17, 号 2, p. 183-190, 発行日 1992-11
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