Loading...
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...
Na minha lista:
| Udgivet i: | Case Rep Genet |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Hindawi
2020
|
| Fag: | |
| Online adgang: | 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 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|