β-Thalassemia is a genetic disorder characterized by reduced or absent synthesis of the beta chains of hemoglobin, leading to ineffective erythropoiesis and severe anemia. Patients with ...

Subjects with microcytic anaemia In subjects with microcytic anaemia and suspected iron deficiency anaemia (IDA) or thalassemia, results of Ret-He and RBC-He results are both decreased if compared ...

Red blood cell distribution width in pediatric microcytic anemias ... stains or dyes Seen in lead poisoning, thalassemia syndromes, or iron deficiency anemia Elliptocyte An oval shaped RBC ...

Sickle cell disease causes red blood cells to become rigid and sickle-shaped, resulting in frequent pain and anemia, while thalassemia causes abnormal hemoglobin due to deficient globin chains. 1 ...

Mitapivat shows promise in treating SCD and thalassemia, with ongoing Phase 3 trials showing positive results for hemoglobin improvement. Expanding Pyrukynd’s label to include pediatric and ...