Sickle cell disease (SCD) stands as one of the most prevalent genetic disorders globally,
characterized by the abnormal hemoglobin S (HbS) leading to distorted erythrocyte …

Abstract Sickle Cell Disease (SCD) is a hereditary hemoglobinopathy characterized by the
aberrant hemoglobin S, resulting in the formation of sickle-shaped red blood cells and a …

Sickle cell anemia (SCA) is a hereditary hemoglobinopathy characterized by the presence of
abnormal hemoglobin S (HbS), leading to the polymerization of red blood cells and the …

Sickle cell anemia (SCA) is a genetic hemoglobinopathy characterized by abnormal
hemoglobin S (HbS) production, leading to the formation of sickle-shaped red blood cells …

Sickle cell disease (SCD) is an inherited hemoglobinopathy affecting millions of people
worldwide. It occurs due to a point mutation in beta-globin chain of hemoglobin (Hb). Sickle …

Sickle cell disease (SCD) embraces a group of genetic hemolytic disorders associated with
high morbidity and mortality. SCD is characterized by a complex pathophysiology initiated …

Sickle cell disease (SCD) is the most severe monogenic hemoglobinopathy caused by a
single genetic mutation that leads to repeated polymerization and depolymerization of …

Sickle cell disease (SCD) is a class of hemoglobinopathy in humans, which causes a
disruption of the normal activities in different systems. Although this disease begins with the …

Abstract Sickle Cell Anemia (SCA) is a hereditary blood disorder characterized by the
presence of abnormal hemoglobin, leading to chronic hemolytic anemia, vaso-occlusive …

Sickle cell disease (SCD) is a genetic disease caused by a single mutation in the β-globin
gene, leading to the production of an abnormal hemoglobin called hemoglobin S (HbS) …