In autosomal recessive inheritance, if both parents are carriers, what is the risk per pregnancy that a sibling is affected?

Prepare for the Clinical Genetics Test. Utilize flashcards and multiple-choice questions, each with hints and explanations. Achieve success on your exam!

Multiple Choice

In autosomal recessive inheritance, if both parents are carriers, what is the risk per pregnancy that a sibling is affected?

Explanation:
When both parents are carriers for an autosomal recessive trait, each pregnancy has the same genotype possibilities: AA (unaffected non-carrier), Aa (carrier), and aa (affected). The cross Aa x Aa yields 1/4 AA, 1/2 Aa, and 1/4 aa. So the chance a pregnancy results in an affected child is 25%, while 50% are carriers and 25% are unaffected non-carriers. The option that gives this full distribution matches the expected probabilities and thus is the best answer.

When both parents are carriers for an autosomal recessive trait, each pregnancy has the same genotype possibilities: AA (unaffected non-carrier), Aa (carrier), and aa (affected). The cross Aa x Aa yields 1/4 AA, 1/2 Aa, and 1/4 aa. So the chance a pregnancy results in an affected child is 25%, while 50% are carriers and 25% are unaffected non-carriers. The option that gives this full distribution matches the expected probabilities and thus is the best answer.

Subscribe

Get the latest from Passetra

You can unsubscribe at any time. Read our privacy policy