Familial chorea and myoclonus epilepsy
Familial chorea and myoclonus epilepsy
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家族性舞蹈病和肌阵挛癫痫
DOI：
10.1212/wnl.28.9.913
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发表时间：
1978
期刊：
影响因子：
9.9
通讯作者：
Hidehiro Suzuki
中科院分区：
文献类型：
--
作者：
N. Takahata;Koichi Ito;Y. Yoshimura;Kyoji Nishihori;Hidehiro Suzuki
家族性疾病的特征是舞蹈病、共济失调、肌阵挛、惊厥、痴呆和智力迟钝。在5例病例中，主要病变累及小脑齿状核，伴有神经细胞丢失、神经胶质增生、染色质溶解和grumose变性。苍白球内可见纤维性胶质细胞增生。
A familial disorder was characterized by chorea, ataxia, myoclonus, convulsions, dementia, and mental retardation. In five cases, the main lesion affected cerebellar dentate nuclei, with nerve cell loss, gliosis, chromatolysis, and grumose degeneration. Fibrous glial cell proliferation was detected in the globus pallidus.