NEET BIOLOGY

GENETICS AND EVOLUTION

GENETIC BASIS OF INHERITANCE

Question [CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
Disorder when blood cells are misshapen, resulting in a decrease of oxygen and caused by a defective allele for a polypeptide in hemoglobin
A
Duschenne’s muscular dystrophy
B
Turner’s Syndrome
C
sickle cell anemia
D
Down Syndrome
Explanation: 

Detailed explanation-1: -Sickle cell anemia is one of a group of inherited disorders known as sickle cell disease. It affects the shape of red blood cells, which carry oxygen to all parts of the body. Red blood cells are usually round and flexible, so they move easily through blood vessels.

Detailed explanation-2: -Sickle cell disease is a hereditary disease seen most often among people of African ancestry. Caused by mutations in one of the genes that encode the hemoglobin protein, the disease is inherited as an autosomal recessive trait. The mutation causes the red blood cells to take on an unusual sickle shape.

Detailed explanation-3: -Poikilocytosis is a term for abnormal-shaped red blood cells in the blood. Poikilocytosis refers to an increase in abnormal red blood cells of any shape that makes up 10% or more of the total population.

Detailed explanation-4: -People with sickle cell disease produce unusually shaped red blood cells that can cause problems because they do not live as long as healthy blood cells and can block blood vessels. Sickle cell disease is a serious and lifelong health condition, although treatment can help manage many of the symptoms.

Detailed explanation-5: -Sickle cell disease is a genetic disorder caused by mutations in the beta globin gene that leads to faulty hemoglobin protein, called hemoglobin S. Hemoglobin S changes flexible red blood cells into rigid, sickle-shaped cells. These sickle cells can block blood flow, and result in pain and organ damage.

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