Investigating the level of Hba1c and insulin level in β-thalassemia patients

Background: β-thalassemia is an inherited blood disorder characterized by reduced or no synthesis of β globin chain, resulting in chronic anemia, so blood transfusion is required as curative therapy. Repeated blood transfusions lead to iron overload that can lead to multiple organ damage, including...

Full description

Bibliographic Details
Main Authors: Husnan Mujiburrahman, Qodri Santosa, Joko Setyono, Nendyah Roestijawati, Lantip Rujito
Format: Article
Language:English
Published: Universitas Muhammadiyah Purwokerto 2023-12-01
Series:Medisains
Subjects:
Online Access:https://jurnalnasional.ump.ac.id/index.php/medisains/article/view/18362