Background Thalassemia is a common disorder worldwide with a predominant incidence in
Mediterranean countries, North Africa, the Middle East, India, Central Asia, and Southeast …

The principal aim of our study was to investigate whether patients transplanted more than 20
years ago for β-thalassemia major had a different health-related quality of life (HRQoL) …

Background Thalassemia is a major health problem that disturbs the lifestyle of the affected
patient. The aim of this work is to detect the impact of thalassemia on the quality of life …

Objectives To assess and compare the Quality of Life (QOL) of children with beta-
thalassemia major on regular transfusion therapy with normal children, and of the caregivers …

Background: Thalassemia is a chronic, inherited blood disorder, which in its most severe
form, causes life-threatening anemia. Thalassemia patients not only engage with difficulties …

Objectives: To assess the health related quality of life (HRQoL) in Iraqi Kurd children and
adolescents with thalassemia, and identify the factors that affect it. Methods: In the period …

Objectives: To assess the quality of life among children and adolescents with thalassemia
major. Methods: his cross-sectional study used the Pediatric Quality of Life Inventory …

Transfusion‐dependent β‐thalassaemia (TDβT) is a genetic disorder characterised by
reduced or absent β‐globin chain synthesis, resulting in chronic anaemia. Treatment …

Abstract Background Thalassemia Major is a preventable genetic disorder characterized by
abnormal hemoglobin synthesis and lifelong blood transfusions. The children suffering from …

Thalassemia is a disorder of hemoglobin (Hb) synthesis characterized by chronic hemolysis.
In β-thalassemias major (β-TM), patients require regular transfusion at an early age due to …