线粒体脑肌病临床表现复杂多样,不易早期诊断,现对线粒体肌病误诊1例分析如下。1病历摘要男,28岁。因反复发作性抽搐6个月,双眼视力下降1个月,加重7 d于2007-01-03入我院。患者于入院前6个月出现反复发作性四肢抽搐伴意识丧失,于我院诊断为癫痫持续状态,入院前5个月再次出现上 The clinical manifestations of mitochondrial encephalomyopathy is complex and diverse, not easy to diagnose early, now a case of mitochondrial myopathy misdiagnosed as follows. 1 medical record summary male, 28 years old. Due to recurrent seizures for 6 months, binocular vision decreased by 1 month, increased 7 d into our hospital from 2007-01-03. Patients in the 6 months before admission recurrent episodes of limbs and convulsions with loss of consciousness in our hospital diagnosed as status epilepticus, 5 months before admission appeared again