[节段性肌张力障碍与线粒体脑肌病]
[Segmental dystonia and mitochondrial encephalomyopathy].
作者信息
Donnet A, Guinot H, Pellissier J F, Desnuelle C, Cozzone P, Bouchacourt M, Khalil R
机构信息
Clinique de Neurologie, CRMBM-CNRS Faculté de Médecine, Marseille.
出版信息
Rev Neurol (Paris). 1992;148(1):51-3.
PMID:1318569
Abstract
A 55 year-old male experienced a dystonia of the right upper limb followed by a ptosis with complete ophthalmoplegia and cataract. He developed a sensory neuropathy and personality changes. Ragged-red fibers were found on muscle biopsy. There was a major defect in complex III and IV activity.
摘要
一名55岁男性先出现右上肢肌张力障碍，随后出现上睑下垂伴完全性眼肌麻痹及白内障。他还出现了感觉神经病变和人格改变。肌肉活检发现破碎红纤维。复合体III和IV活性存在严重缺陷。
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