线粒体—脂类—糖元病(mitochondrial-lipid-glycogen disease),即线粒体肌病(mitochondrialmyopathy),为一罕见疾病,复习文献,尚未见到有合并房间隔缺损的报告,现将我们遇到的一例报告如下。 病例报告 女性,16岁,住院号62666。因四肢无力3年于85年5月9日收我科。病人于82年始四肢无力,以双下肢为重,呈持续性,活动受限,且活动时伴心悸及面色苍白,病情进行性加重,无肌肉疼痛,肌束震颤 Mitochondrial-lipid-glycogen disease, mitochondrialmyopathy, is a rare disease, review of literature, have not yet seen a report of atrial septal defect, now we encounter A case report is as follows. Case report Female, 16 years old, hospital number 62666. Due to limb weakness 3 years in May 9, 85 received my subjects. The patient started to have weakness in both limbs in 82 years, with persistent lower extremities, limited mobility, palpitations and pale skin during the activity, progressive exacerbations, no muscle pain and tremor