肌红蛋白尿
磷酸甘油酸变位酶
医学
肌肉痉挛
内科学
内分泌学
化学
糖酵解
新陈代谢
横纹肌溶解症
作者
Shin J. Oh,Kyung‐Seok Park,Hewitt F. Ryan,Moris J. Danon,Jiesheng Lu,Ali Naini,Salvatore DiMauro
摘要
Abstract We report two patients in whom phosphoglycerate mutase (PGAM) deficiency was associated with the triad of exercise‐induced cramps, recurrent myoglobinuria, and tubular aggregates in the muscle biopsy. Serum creatine kinase (CK) levels were elevated between attacks of myoglobinuria. Forearm ischemic exercise tests produced subnormal increases of venous lactate. Muscle biopsies showed subsarcolemmal tubular aggregates in type 2 fibers. Muscle PGAM activities were markedly decreased (3% of the normal mean) and molecular genetic studies showed that both patients were homozygous for a described missense mutation (W78X). A review of 15 cases with tubular aggregates in the muscle biopsies from our laboratory and 15 cases with PGAM deficiency described in the literature showed that this clinicopathological triad is highly suggestive of PGAM deficiency. Muscle Nerve, 2006
科研通智能强力驱动
Strongly Powered by AbleSci AI