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: | , , , , , |
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| Formato: | article |
| Lenguaje: | EN FA |
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Babol University of Medical Sciences
2012
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| Materias: | |
| Acceso en línea: | https://doaj.org/article/d9f25c1454934af5b06acb0f629503fa |
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