线粒体脑肌病
乳酸性酸中毒
线粒体脑肌病
症候群
医学
线粒体肌病
肾功能
内科学
急性肾损伤
急性肾小管坏死
病理
心脏病学
线粒体DNA
生物
遗传学
基因
作者
Fred H. Hsieh,Reginald Gohh,Lance D. Dworkin
摘要
Melas (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes) is one of a group of heterogeneous yet clinically distinct syndromes ascribed to a defect in mitochondrial function. Here, the case of a patient diagnosed with the MELAS syndrome who subsequently developed acute renal failure is reported. Although no clear renal insult was evident at the time, the clinical picture was consistent with the diagnosis of acute tubular necrosis. The patient's renal function subsequently returned to baseline. This article reviews the literature concerning renal involvement in the mitochondrial encephalomyopathies, including MELAS, and proposes a mechanism by which patients suffering from mitochondrial disorders may be more susceptible to renal hypoxic injury and acute renal failure.
科研通智能强力驱动
Strongly Powered by AbleSci AI