Abstract:Background: Beta-thalassemia syndromes are a set of hereditary blood disorders marked by a deficiency of betaglobin chain synthesis, resultant in decrease hemoglobin in red blood cells [RBC], anemia, and a reduced RBC production Aim of the work: To evaluate glycometabolic and liver function in cases with β-thalassemia major and their correlation with serum iron and ferritin Patients and methods: This was a case-control study that was performed in the pediatric department of Al-Azher University Hospital in Dami… Show more
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