Hematological Alterations among Sickle Cell Disease Patients in Steady State and Their Clinical Implications
Amusan Festus Olatubosun, Ugbomoiko Daniel Ohilebo, Obhioze Augustine Akpoka, Adesina Beatrice Ebun, Oniye Adesola Helen & Erameh Theophilus Ogie · Journal of Scientific Research and Reports · 2025
Introduction: In sub-Saharan Africa, sickle cell disease (SCD) is a common genetic hemoglobinopathy that is typified by vaso-occlusive crises and chronic hemolytic anemia. Even if they are less severe, hematological changes in steady state—defined as no crisis, transfusion, or in...