Bermils C, Tassin S, Brucher J M, de Barsy T
Neurology. 1983 Dec;33(12):1613-5. doi: 10.1212/wnl.33.12.1613.
The case of an adolescent with idiopathic recurrent myoglobinuria is reported. The following features are emphasized: (1) persistence of limb weakness and elevated CK levels between the attacks, (2) a constant myopathic pattern in EMG, and (3) chronic morphologic abnormalities of myopathy in two muscle biopsies. All known causes of myoglobinuria were investigated and ruled out.
报告了一例患有特发性复发性肌红蛋白尿的青少年病例。强调了以下特征：（1）发作期间肢体无力持续存在且肌酸激酶水平升高；（2）肌电图呈现持续的肌病模式；（3）两次肌肉活检显示存在慢性肌病形态学异常。对所有已知的肌红蛋白尿病因进行了调查并排除。
