Department of Neurological Sciences and Vision, Section of Neurology, University of Verona, 37134 Verona, Italy.
Neuromuscul Disord. 2009 Nov;19(11):776-8. doi: 10.1016/j.nmd.2009.08.007. Epub 2009 Sep 23.
Phosphoglycerate mutase (PGAM) deficiency causes a rare metabolic myopathy characterized by exercise-related myalgia and myoglobinuria. This disorder was described in 13 patients and five different mutations in the PGAM-M gene were identified. We report on a new patient with an unusual clinical presentation. As a youth, he participated in different sports without complaining of muscular symptoms, but at 44 years of age, after a brief, intense effort, he experienced lightheadedness without fainting. Serum CK was elevated and the ischemic exercise test showed a pathological lactate response. Muscle biopsy showed only mild abnormalities, but biochemical study revealed a defect of PGAM and genetic analysis showed two different mutations in the PGAM-M gene. Our case expands the clinical spectrum of PGAM deficiency and suggests that the frequency of this metabolic myopathy may be underestimated.
磷酸甘油酸变位酶(PGAM)缺乏症导致一种罕见的代谢性肌病,其特征为与运动相关的肌肉疼痛和肌红蛋白尿。该疾病已在 13 名患者中进行了描述,并鉴定了 PGAM-M 基因中的 5 种不同突变。我们报告了一位具有不典型临床表现的新患者。在青年时期,他参加了不同的运动,没有出现肌肉症状,但在 44 岁时,在短暂而剧烈的运动后,他出现了头晕但没有晕厥。血清肌酸激酶升高,缺血运动试验显示出异常的乳酸反应。肌肉活检仅显示轻度异常,但生化研究显示 PGAM 缺陷,基因分析显示 PGAM-M 基因中有两种不同的突变。我们的病例扩展了 PGAM 缺乏症的临床谱,并表明这种代谢性肌病的频率可能被低估了。