An elderly diabetic patient with McArdle disease and recurrent rhabdomyolysis: a potential association with late hypoinsulinemia?

BACKGROUND: McArdle disease is a myopathy caused by mutations in PYGM gene that is characterized by reduced or absent activity of myophosphorylase. Reports of patients with concomitant McArdle disease and diabetes are scarce. We report a case of a patient with a late diagnosis of McArdle disease and...

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Detalles Bibliográficos
Autores principales: Chocair, Pedro Renato, Mohrbacher, Sara, de Menezes Neves, Precil Diego Miranda, Pereira, Leonardo Victor Barbosa, Oliveira, Erico Souza, Nardotto, Luciana Loureiro, Bales, Alessandra Martins, Sato, Victor Augusto Hamamoto, Silva, Sabrina Neves, Ferreira, Bernadete Maria Coelho, Cuvello-Neto, Américo Lourenço
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644386/
https://www.ncbi.nlm.nih.gov/pubmed/33153458
http://dx.doi.org/10.1186/s12877-020-01812-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644386/
https://www.ncbi.nlm.nih.gov/pubmed/33153458
http://dx.doi.org/10.1186/s12877-020-01812-4

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