PATHOLOGY

PATHOLOGY MCQ

GENETICS AND DISEASE

Question [CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
A child is diagnosed with a rare disease. Neither parent has the disease. How did the child inherit the disorder?
A
The disorder is dominant and carried by a parent.
B
The disorder is recessive and carried by both parents.
C
The disorder is sex-linked and inherited only from the father.
D
A mutation in the child occurred.
Explanation: 

Detailed explanation-1: -Dominant means only one parent needs to pass along the abnormal gene in order to produce the disorder. In families where one parent carries a defective gene, each child has a 50 percent chance of inheriting the gene and therefore the disorder.

Detailed explanation-2: -Recessive inheritance means both genes in a pair must be abnormal to cause disease. People with only one defective gene in the pair are called carriers. These people are most often not affected with the condition. However, they can pass the abnormal gene to their children.

Detailed explanation-3: -Dominant genetic diseases are caused by a mutation in one copy of a gene. If a parent has a dominant genetic disease, then each of that person’s children has a 50% chance of inheriting the disease. Dominant diseases can also occur spontaneously; this happens when a random mutation in one gene occurs at conception.

There is 1 question to complete.