Sengers R C, Stadhouders A M, Jaspar H H, Lamers K J, Trijbels J M, Notermans S L
Eur J Pediatr. 1980 Aug;134(2):161-5. doi: 10.1007/BF01846039.
Myophosphorylase deficiency (McArdle's syndrome) is an uncommon condition characterized by exercise intolerance, muscle cramps and myoglobinuria. The present report describes the clinical, histochemical, electronmicroscopic and biochemical findings in a 12-year-old boy with myophosphorylase deficiency. The diagnosis should have been suspected when the boy was 6 years old. Most index cases have not been diagnosed until adult life, but this syndrome has to be considered in the differential diagnosis of exercise intolerance in childhood.
肌磷酸化酶缺乏症(麦卡德尔综合征)是一种罕见病症,其特征为运动不耐受、肌肉痉挛和肌红蛋白尿。本报告描述了一名患有肌磷酸化酶缺乏症的12岁男孩的临床、组织化学、电子显微镜及生化检查结果。该男孩6岁时就应怀疑此病。多数典型病例直到成年才得以诊断,但在儿童运动不耐受的鉴别诊断中必须考虑到这种综合征。