McArdle disease: a case report and review

McArdle disease (glycogen storage disease type V) is a pure myopathy caused by an inherited deficit of myophosphorylase. The disease exhibits clinical heterogeneity, but patients typically experience exercise intolerance, acute crises of early fatigue, and contractures, sometimes with rhabdomyolysis...

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Detalles Bibliográficos
Autores principales: Leite, Alberto, Oliveira, Narciso, Rocha, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658246/
https://www.ncbi.nlm.nih.gov/pubmed/23754915
http://dx.doi.org/10.2147/IMCRJ.S28664

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658246/
https://www.ncbi.nlm.nih.gov/pubmed/23754915
http://dx.doi.org/10.2147/IMCRJ.S28664

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