麦卡德尔病:临床回顾及病例报告。

Bradley R Keel, Michael Brit
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引用次数: 0

摘要

麦卡德尔氏病是一种罕见的糖原疾病,涉及肌肉磷酸化酶缺乏。这种缺乏可导致横纹肌溶解和随后的肾功能衰竭。mccardle病的表现与其他代谢性肌病相似,伴有运动性疲劳、肌痛、虚弱或原因不明的横纹肌溶解。出现无法解释的症状时应提出怀疑,并可进行肌肉活检以确认诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
McArdle's disease: a clinical review and case report.

McArdle's Disease is a rare glycogen disease involving deficiency in muscle phosphorylase. This deficiency can lead to rhabdomyolysis and subsequently renal failure. McArdle's Disease has a similar presentation as several other metabolic myopathies with exercise-induced fatigue, myalgias, weakness or unexplained rhabdomyolysis. Suspicion should be raised in the presence of unexplained symptoms, and muscle biopsy can be done to confirm the diagnosis.

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