Chargement en cours...
Anesthetic management of a patient with sickle β(+) thalassemia
Sickle cell disease is a congenital condition and its most common clinical manifestation is anemia due to chronic hemolysis. Persistent and accelerated hemolysis associated with multiple transfusions is a recognized risk factor for the development of cholelithiasis. The occurrence of gallstones is o...
Enregistré dans:
| Auteurs principaux: | , , , |
|---|---|
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Medknow Publications
2011
|
| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3101768/ https://ncbi.nlm.nih.gov/pubmed/21655030 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1658-354X.76496 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|