Very-Long-Chain Acyl-Co-Enzyme A Dehydrogenase Deficiency Presenting as Rhabdomyolysis: First Case Report from Sri Lanka

BACKGROUND: Rhabdomyolysis can be either inherited or acquired such as in metabolic myopathies. Very-long-chain acyl-CoA dehydrogenase deficiency is a rare fatty acid oxidation disorder which presents with different phenotypes, and the mild adult form can present as intermittent rhabdomyolysis. Here...

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Bibliografische gegevens
Gepubliceerd in:Case Rep Genet
Hoofdauteurs: Wijayabandara, Maheshi, Gamakaranage, Champika, Hettiarachchi, Dineshani
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Hindawi 2020
Onderwerpen:
Case Report
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7578713/
https://ncbi.nlm.nih.gov/pubmed/33110664
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/8894518
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