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Successful reversal of propionic acidaemia associated cardiomyopathy: Evidence for low myocardial coenzyme Q(10) status and secondary mitochondrial dysfunction as an underlying pathophysiological mechanism

机译:丙酸血症相关性心肌病的成功逆转:低心肌辅酶Q(10)状态和继发性线粒体功能障碍作为基础病理生理机制的证据

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摘要

Dilated cardiomyopathy is a rare complication in propionic acidaemia (PA). Underlying pathophysiological mechanisms are poorly understood.
机译:扩张型心肌病是丙酸血症(PA)的罕见并发症。根本的病理生理机制了解甚少。

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