- McArdle's disease: a clinical review and case report.
McArdle's disease: a clinical review and case report.
Tennessee medicine : journal of the Tennessee Medical Association (2013-11-29)
Bradley R Keel, Michael Brit
PMID24282836
摘要
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.