| 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 |
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|
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
Nakamura, Kimi
Yanai, Mika
Tsuruta, Chihiro
Iida, Masashi
Hanada, Masanori
|
| 言語 |
|
|
言語 |
eng |
| キーワード |
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|
主題 |
chorea, family history, dentatoruburopallidoluysian atrophy, caudate nucleus, cerebral white matter |
| 内容記述 |
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|
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 |
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|
出版者 |
The Kinki University Medical Association |
|
言語 |
en |
| 資源タイプ |
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|
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 |
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収録物識別子タイプ |
PISSN |
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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
|