Rhabdomyolysis and Exercise Intolerance in a 45-Year-Old Man

Humzah Ahmad, Malvika Govil, Salman Bhai, Chunyu Cai
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Abstract

A 45-year-old man presented to neuromuscular clinic after a first-time episode of non-traumatic rhabdomyolysis after aerobic exercise. Prior to his diagnosis, he had an extensive medical workup to evaluate for elevated transaminases and creatinine, including liver and renal biopsies. On history, the patient confirmed a lifelong history of exercise intolerance. Creatine kinase evaluation revealed an elevated baseline value. Genetic testing disclosed homozygous variants of uncertain significance and required exercise testing and muscle biopsy to identify the underlying etiology. This case demonstrates pitfalls of genetic testing and an approach to identify this form of myopathy.
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一名 45 岁男子的横纹肌溶解症和运动不耐受症
一名 45 岁男子在有氧运动后首次出现非创伤性横纹肌溶解症,随后来到神经肌肉诊所就诊。确诊前,他接受了广泛的医学检查,以评估转氨酶和肌酐是否升高,包括肝脏和肾脏活检。根据病史,患者证实终生患有运动不耐受症。肌酸激酶评估显示基线值升高。基因检测发现了意义不确定的同基因变异,需要进行运动测试和肌肉活检来确定潜在病因。本病例展示了基因检测的误区和识别这种肌病的方法。
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