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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Autores principales: Basma Matar, Magdy Sakr, Lotfy Alsehaimy, Hesham Abd al-samee
Formato: article
Lenguaje:EN
Publicado: Al-Azhar University, Faculty of Medicine (Damietta) 2021
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Acceso en línea:https://doaj.org/article/bcdd71df38ec4889bfe1c1ffeadfd5ac
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