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査読

39 被引用数 (Scopus)

抄録

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.

本文言語英語
ページ(範囲)1395-1399
ページ数5
ジャーナルNeurology
32
12
DOI
出版ステータス出版済み - 12 1982
外部発表はい

All Science Journal Classification (ASJC) codes

  • 臨床神経学

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