Comparison of Need of Transfusion and Adverse Effects before and after Splenectomy in Beta-Thalassemic Patients

BACKGROUND AND OBJECTIVE: Thalassemia is the most common hereditary disease. Hypersplenism and splenomegaly occur in thalassemic patients due to the hereditary defect in globin chain of hemoglobin molecule and extramedullary hematopoiesis that results in more destruction in red blood cells. Therefor...

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Autores principales: AA Darzi, A Tamaddoni, MS Ramezani, L Ramezani, F Gharghabi, N Soleymanpour
Formato: article
Lenguaje:EN
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Publicado: Babol University of Medical Sciences 2012
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Acceso en línea:https://doaj.org/article/d9f25c1454934af5b06acb0f629503fa
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