A Case Report of McArdle Disease Diagnosed Following Statin-Induced Myositis

McArdle disease is a rare condition, characterized by a deficiency of phosphorylase muscle isoform, an enzyme responsible for the breaking down of glycogen, necessary for obtaining energy. Patients typically present with exercise intolerance, myalgias, fatigue, cramps, muscle stiffness, and/or weakn...

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Detalles Bibliográficos
Autores principales: Teles, João S, Ramos, Catarina T, Almeida, Beatriz M, Sousa, Anabela V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Family/General Practice
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552332/
https://www.ncbi.nlm.nih.gov/pubmed/37809236
http://dx.doi.org/10.7759/cureus.44701

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552332/
https://www.ncbi.nlm.nih.gov/pubmed/37809236
http://dx.doi.org/10.7759/cureus.44701

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