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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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| Vydáno v: | EXCLI J |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Leibniz Research Centre for Working Environment and Human Factors
2020
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| Témata: | |
| On-line přístup: | 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 |
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