Evaluation Of Iron Overload Approach in Thalassemia Patients at The Thalassemia Center

Abstract excerpt

<h4>Background: </h4> Thalassemia is a genetic blood disorder as a result of a defect in the genes responsible for the production of globin chains in hemoglobin, which is responsible for transporting oxygen to the cells of the body. Iron buildup is common in thalassemia patients as a result of frequent blood transfusions or because of the disease itself. The objectives of this research depend on the approach of ir...

Topics

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• beta-Globins
• beta-Thalassemia
• Clinical Decision-Making
• Combined Modality Therapy
• Disease Management
• Disease Susceptibility
• Incidence
• Severity of Illness Index

Identifiers and source

Literature Corpus work

c5139d44-d353-509a-b5b1-a5b0029b9e40

DOI

10.21203/rs.3.rs-2669530/v1