Answer:
here.
Explanation:
Due to the prevalence of malaria in Africa, the allele for sickle cell anemia (HbS) provides a selective advantage. That's why it remains in the population.
A normal African person (HbAHbA), with normal haemoglobin, will not die of anemia, but will die of malaria.
An African person with sickle cell anemia (HbSHbS), with abnormal haemoglobin, will die of anemia.
A heterozygous African person (HbAHbS), with half of his red blood cells (RBCs) being normal and the other half being sickle-shaped, will neither die from anemia, nor malaria since the plasmodium will be incapable of completing its life cycle in the abnormal RBCs.
Thus heterozygous African people will grow, reproduce and pass on the HbS allele to the next generations.
