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...

Cur síos iomlán

Na minha lista:
Sonraí Bibleagrafaíochta
Foilsithe in:EXCLI J
Main Authors: Schnedl, Wolfgang J., Schenk, Michael, Enko, Dietmar, Mangge, Harald
Formáid: Artigo
Teanga:Inglês
Foilsithe: Leibniz Research Centre for Working Environment and Human Factors 2020
Ábhair:
Case Report
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC7590829/
https://ncbi.nlm.nih.gov/pubmed/33122977
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.17179/excli2020-2866
Clibeanna: Cuir Clib Leis
Gan Chlibeanna, Bí ar an gcéad duine leis an taifead seo a chlibeáil!

Míreanna Comhchosúla