Unusual form of cerebellar ataxia
Unusual form of cerebellar ataxia
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不寻常形式的小脑性共济失调
DOI：
10.1212/wnl.8.3.205
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发表时间：
1958
期刊：
影响因子：
9.9
通讯作者：
N. Malamud
中科院分区：
文献类型：
--
作者：
James K. Smith;V. E. Gonda;N. Malamud
小脑性共济失调包括多种疾病。它们可分为 Menzel 的遗传性脊髓小脑型、Holmes 的遗传性小脑-橄榄变性和 D6jerine-Thomas 的散发性橄榄脑桥小脑萎缩。然而，很少观察到齿状-红脑系统的主要受累，这就是报告以下病例的原因。该病例的其他有趣特征是小脑和锥体外系的联合变性以及巴宾斯基小脑僵住征的不寻常发生。
INCLUDED in the group of cerebellar ataxias is a great variety of disorders. They may be classified into the hereditary spinocerebellar form of Menzel, the hereditary cerebello-olivary degeneration of Holmes, and the sporadic olivopontocerebellar atrophy of D6jerine-Thomas.’ Predominant involvement of the dentato-rubral system has rarely been observed, however, and that is why the following case is reported. Other features of interest in this case were combined degeneration of cerebellar and extrapyramidal systems and the unusual occurrence of Babinski’s sign of cerebellar catalepsy.