McArdle disease in a patient with anorexia nervosa: a case report

BACKGROUND: McArdle disease is an autosomal recessive genetic disorder caused by a deficiency of the glycogen phosphorylase (myophosphorylase) enzyme, which muscles need to break down glycogen into glucose for energy. Symptoms include exercise intolerance, with fatigue, muscle pain, and cramps being...

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Detalles Bibliográficos
Autores principales: Dalle Grave, Riccardo, Patacca, Enrico, Conti, Maddalena, Soave, Fabio, Dametti, Laura, Dalle Grave, Anna, Calugi, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308889/
https://www.ncbi.nlm.nih.gov/pubmed/35871462
http://dx.doi.org/10.1007/s40519-022-01451-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308889/
https://www.ncbi.nlm.nih.gov/pubmed/35871462
http://dx.doi.org/10.1007/s40519-022-01451-1

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