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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
ZUSAMMENFASSUNG

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.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

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