Dentatorubro-pallidoluysian degeneration: Clinical, neuro-ophthalmologic, biochemical, and pathologic studies on autosomal dominant form

Ikuo Goto, Shozo Tobimatsu, Michiya Ohta, Shinichi Hosokawa, Hiroshi Shibasaki, Yoshigoro Kuroiwa

研究成果: Contribution to journalArticle

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抜粋

Four cases in two generations of a Japanese family are described as affected by an autosomal dominant-inherited cerebellar ataxia, pyramidal and extrapyramidal signs, and abnormal ocular movements, resembling Machado-Joseph disease. The neuro-ophthalmologic examination suggests the involvement of multiple motor control systems. The neuropathologic examination of one case showed neuronal loss in the subthalamic nuclei, pallidum, dentate nuclei of cerebellum, and red nuclei, which is distinct from Machado-Joseph disease.

元の言語英語
ページ(範囲)1395-1399
ページ数5
ジャーナルNeurology
32
発行部数12
DOI
出版物ステータス出版済み - 12 1982

All Science Journal Classification (ASJC) codes

  • Clinical Neurology

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