Evaluation of Serum Insulin, Glucose and Liver Function in β-Thalassemia Major and Their Correlation with Iron Overload
Background: Beta-thalassemia syndromes are a set of hereditary blood disorders marked by a deficiency of beta-globin 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 case...
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Formato: | article |
Lenguaje: | EN |
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Al-Azhar University, Faculty of Medicine (Damietta)
2021
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Acceso en línea: | https://doaj.org/article/bcdd71df38ec4889bfe1c1ffeadfd5ac |
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