Background: Thalassemia major is a chronic disease in children that harms children quality
of life by interrupting physical function, emotional function, social function, and school …

Background: Patients with β-thalassemia major (BTM) had variable prevalence of
undernutrition and abnormal body composition. Methods: We performed an electronic …

Background Beta thalassemia major (TM) is the most common inherited genetic disorder
worldwide. Patients are at risk of iron overload, which leads to various forms of tissue …

Background. Thalassemia is one of the most common genetic hematologic disorders in the
world. Despite outstanding achievements in prenatal diagnosis and a decrease in the …

Health‐related quality of life (HRQOL) is a patient‐reported outcome that assesses the
impact of a disease or illness on different domains of a patient's life. Different general and …

Background Transfusion-dependent β-thalassemia (TDT) is a hereditary blood disorder that
often leads to complications affecting growth, nutritional status, and muscle mass in children …

Talasemia adalah kelainan gen tunggal resesif autosom akibat ketidakseimbangan
produksi rantai globin, yaitu rantai globin-α dan globin-β yang hingga kini kasusnya …

The purpose of this review is to summarize the recent knowledge that has been gathered,
allowing a better understanding of iron status in children with thalassemia. Children with …

In recent years, a multitude of studies have been conducted to investigate the assessment of
quality of life (QoL) among individuals affected by thalassemia. This sco** review aimed to …

Background Allogeneic hematopoietic stem cell transplantation (allo-HSCT) has proven to
be an effective curative intervention for children with β-thalassemia major (β-TM). They are …