Severe rhabdomyolysis in homozygote carnitine palmitoyltransferase II deficiency

Carnitine palmitoyltransferase II (CPT II) deficiency represents an inherited defect in mitochondrial long-chain fatty acid oxidation. Rhabdomyolysis with necrosis of muscle is caused by the destruction of skeletal muscle and leads to systemic, multiorgan complications due to the release of intracel...

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Detalles Bibliográficos
Autores principales: Schnedl, Wolfgang J., Schenk, Michael, Enko, Dietmar, Mangge, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590829/
https://www.ncbi.nlm.nih.gov/pubmed/33122977
http://dx.doi.org/10.17179/excli2020-2866

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590829/
https://www.ncbi.nlm.nih.gov/pubmed/33122977
http://dx.doi.org/10.17179/excli2020-2866

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