You are studying cystic fibrosis (CF). While looking at a pedigree, you notice that the CF phenotype is not present in a set of parents, but one out of their five children has CF. What can you conclude about CF?

Question

Leonard Newman

Biology

31 October, 06:40

You are studying cystic fibrosis (CF). While looking at a pedigree, you notice that the CF phenotype is not present in a set of parents, but one out of their five children has CF. What can you conclude about CF?

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Answers (1)

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Butler · Answer 1

Cystic fibrosis (CF); Genotype cc has CF because it is homozygous recessive.

Explanation:

1. Cystic fibrosis (CF); it is an autosomal recessive disease.

2. As given here, that both the parents are normal but their one out of five children has CF, so we can say that both the parents are carrier for CF,

3. So their genotype is: Cc and Cc.

4. In Cc and Cc; C is dominant over c, and genotype cc is for CF.

cross between both parents; results into progeny: CC, Cc, Cc and cc.

Genotype cc has CF because it is homozygous recessive.