Anemia

Their bites are painful and cause significant blood loss with repeated/heavy exposure, contributing to anemia in livestock and occasionally humans.

Anemia

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Study material on Anemia

Practice questions on Anemia

A 22-year-old woman has a congenital anemia. She has required multiple transfusions of red blood cells for many years. She now has a darker bronze colour to her skin on physical examination. Which of the following microscopic findings would most likely present in her liver?

Answer: C. There is 250 mg of iron in each unit of blood. The body has no mechanism for getting rid of excess iron. A small amount of iron is lost with normal desquamation of epithelia, and menstruating women will lose a bit more. The excess iron becomes storage iron, or hemosiderin. Over time, hemosiderosis involves more and more tissues of the body, particularly the liver, but also skin (bronze colour), heart (with heart fail

In a population, 4% have sickle cell anemia. What percentage is heterozygous (advantageous to malaria)?

Answer: E. If q² = 0.04, then q = 0.2 and p = 0.8. Heterozygous frequency = 2pq = 2(0.8)(0.2) = 0.32 or 32%. ---

What selection type fits sickle cell anemia?

Answer: A. Sickle cell anemia represents balancing/stabilizing selection where heterozygotes have a survival advantage (malaria resistance) maintaining both alleles in the population. ---

In a certain group of African people, 4 percent are born with sickle cell anemia. What percentage of the group has the selective advantage of being more resistant to malaria than those individuals who are homozygous for normal hemoglobin or for sickle cell anemia?

Answer: B. If 4% have sickle cell anemia (ss), then q² = 0.04, so q = 0.2 and p = 0.8. Heterozygotes (Ss) have malaria resistance: 2pq = 2(0.8)(0.2) = 0.32 = 32%. ---

Which selection type fits sickle cell anemia?

Answer: A. Sickle cell anemia shows balancing selection (a type of stabilizing selection) where heterozygotes have an advantage (malaria resistance) over both homozygotes. ---

Blood is drawn from a child with severe anemia and the hemoglobin protein is degraded for peptide and amino acid analysis. Of the results below, which change in hemoglobin primary structure is most likely to correlate with the clinical phenotype of anemia?

Answer: A. This substitution pattern (glutamate → valine) matches the classic sickle cell disease mutation at position 6 of the β-globin chain (HbS). ---

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