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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...

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Detalles Bibliográficos
Autores principales: Bharati, Saswata, Das, Subhabrata, Majee, Prasenjit, Mandal, Subrata
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101768/
https://www.ncbi.nlm.nih.gov/pubmed/21655030
http://dx.doi.org/10.4103/1658-354X.76496