Anaemia is a common health problem worldwide that disproportionately affects vulnerable
groups, such as children and expectant mothers. It has a variety of underlying causes, some …

Thalassemia represents one of the most common genetic disorders worldwide,
characterized by defects in hemoglobin synthesis. The affected individuals suffer from …

Background Hemoglobinopathies, the most common inherited blood disorder, are frequently
underdiagnosed. Early identification of carriers is important for genetic counseling of …

Thalassemia is a heritable blood disorder which is the outcome of a genetic defect causing
lack of production of hemoglobin polypeptide chains. However, there is less understanding …

Thalassemia, a genetic blood disorder, stems from faulty synthesis of a-or ß-globin subunits
of hemoglobin, resulting in chronic hemolytic anemia. Diagnosis via complete blood cell …

Hemoglobinopathies are a group of disorders in which the hemoglobin molecule has
abnormal production or structure. The hemoglobin molecules in red blood cells (RBC) are …

Haemoglobinopathies indicate a group of monogenic disorders. The prevalence of
Haemoglobinopathies differs based on geographical regions and is higher in tropical …

A collection of blood illnesses affecting red blood cells are called hemoglobinopathies.
Hemoglobin, a protein found in blood cells, transports oxygen throughout the body and …