Polydactyly is an autosomal dominant disorder A man who is h

Polydactyly is an autosomal dominant disorder. A man who is homozygous for polydactyly has an extra digit on his left hand. His spouse has a normal genotype and phenotype regarding polydactyly. At the population level, this trait is 50% penetrant among heterozygotes. Which of the following is correct regarding their children? Select ALL that apply.

a)the probability that each of their children will be affected is 1 in 4.

b) If their first child is affected, then if they have another child, it is not expected to be affected.

Solution

b) If their first child is affected, then if they have another child, it is not expected to be affected ----> TRUE (because 50% of the offspring are likely to be affected)

e) The probability that each of their children will be affected is 1 in 2. ---> TRUE

Assume that the gene coding for polydactyly is A and the gene coding for normal phenotype is, a; A is dominant over a. Given that the father is homozygous dominant (AA) and the mother is homozygous recessive (aa). And the gene penetration is 50% in heterozygotes.

Cross between them will have the progeny with the following genotypes:

AA* aa -à Aa (All heterozygous).

As the penetrance is 50%, the chances of each child to be affected is 50% or 1 in 2.

Polydactyly is an autosomal dominant disorder. A man who is homozygous for polydactyly has an extra digit on his left hand. His spouse has a normal genotype and

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