Hemoglobin-S- ?-Thalassemia

Hemoglobin S-?-thalassemia is one of the hemoglobinopathies (hemoglobinopathies) and leads to symptoms of sickle cell disease are similar, but less pronounced with those. Because of the increased frequency of hemoglobin-S- as well as ?-thalassemia genes in the same population group, the inheritance of both defects is relatively common. Clinically, the disease leads to symptoms of moderate anemia with signs of sickle cell disease, but occur less frequently and are less…

September 3, 2018