Sickle Cell Anemia Research
Introduction Sickle cell anemia (SCD) is an “autosomal recessive inherited hemoglobinopathy” that causes vaso-occlusive crises and hemolysis due to an abnormal substitution of amino and glutamic acids on the β-globin chain (Keikhaei, Yousefi, & Bahadoram, 2016, p. 252). Nowadays, hydroxyurea (HU) remains the only method that helps alleviate the symptoms...