Carnitine palmitoyltransferase-II deficiency: case presentation and review of the literature
Carnitine palmitoyltransferase-II deficiency, an autosomal recessive disorder, is the most common cause of recurrent rhabdomyolysis in adults. Recognition and avoidance of triggers, such as heavy exercise and stress, is key in prevention of further episodes; however, even with preventative measures,...
Enregistré dans:
| Auteurs principaux: | , |
|---|---|
| Format: | article |
| Langue: | EN |
| Publié: |
Sciendo
2021
|
| Sujets: | |
| Accès en ligne: | https://doaj.org/article/54e9a29cbb3a4ba9b08e85c602d0b9b7 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|