Sickle cell disease is characterized by abnormal hemoglobin HB-S and sickled cells that rupture easily.
Sickle cell disease is characterized by an abnormal kind of hemoglobin HB-S and sickled cells rupture easily. In sickle cell disease, when individuals inherit a mutated gene (hemoglobin with a sickled erythrocyte variety, HbS) from both parents, it leads to the development of the disease.
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