ロード中...
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...
保存先:
| 出版年: | Case Rep Genet |
|---|---|
| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Hindawi
2020
|
| 主題: | |
| オンライン･アクセス: | 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 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|