Evaluation of Hepatic Enzymes in major β-thalassemic Patients using Deferasirox

Abstract β-thalassemia major is a genetic disease that causes sever defect in normal hemoglobin synthesis. The patients with β-thalassemia major need periodic blood transfusions that can result in accumulation of body iron, so treatment with iron chelating agent is required. Complications of this...

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Bibliographic Details

Published in:	Iraqi Journal of Pharmaceutical Sciences
Main Authors:	Ahmed Yahya Dallal Bashi, Fatimah Haitham Fathi
Format:	Article
Language:	English
Published:	College of Pharmacy University of Baghdad 2022-12-01
Subjects:	?-thalassemia Alanine_aminotransferase aspartate aminotransferase alkaline phosphatase ferritin
Online Access:	https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/1605