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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wijayabandara, Maheshi, Gamakaranage, Champika, Hettiarachchi, Dineshani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7578713/
https://www.ncbi.nlm.nih.gov/pubmed/33110664
http://dx.doi.org/10.1155/2020/8894518

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7578713/
https://www.ncbi.nlm.nih.gov/pubmed/33110664
http://dx.doi.org/10.1155/2020/8894518

Ejemplares similares