Abstract β‐thalassemia major is an inherited hemoglobinopathy that requires lifelong red
blood cell transfusions and iron chelation therapy to prevent complications due to iron …

Beta-thalassaemia causes defective haemoglobin synthesis leading to ineffective
erythropoiesis, chronic haemolytic anaemia, and subsequent clinical complications. Blood …

Background: Blood transfusion is a traditional treatment for β-thalassemia (β-thal) that
improves the patients' anemia and lifespan, but it may lead to iron overload in parenchymal …

Thalassemias are a group of congenital hemoglobin (Hb) disorders distinguished by
dwindling or total curtailment of production of one or more globin chains of hemoglobin …

Among the difficulties of living with β-thalassemia, patients frequently require blood
transfusions and experience iron overload. As serum ferritin (SF) provides an indication of …

Beta thalassemia (β-thalassemia) is part of a group of inherited hemoglobinopathies caused
by a mutation in the beta globin gene, leading to minimal functional hemoglobin and …

Background Patients with β-thalassemia major (β-TM), predominantly adult patients, are
associated with physical, mental, and social problems, that result in decreased quality of life …

Thalassemia is the most common monogenic hematologic disease that affects millions in the
world and kills thousands of patients every year. Without transfusion or transplantation …

Abstract Objectives To evaluate the Quality of life (QoL) and the factors affecting it in
transfusion-dependent thalassemic children. Methods Current study was conducted at …

Background Beta‐thalassaemia is an inherited blood disorder that reduces the production of
haemoglobin. The most severe form requires recurrent blood transfusions, which can lead to …