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Merck

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
ABSTRAKT

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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Sigma-Aldrich
Phosphorylase b from rabbit muscle, lyophilized powder, ≥20 units/mg protein, 2× crystallization
Sigma-Aldrich
Phosphorylase b from rabbit muscle, For use as a marker in SDS-PAGE