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Two heterozygous carriers (Cc) of cystic fibrosis. Percent of offspring who are carriers but not affected?

  1. A
    0%
  2. B
    25%
  3. C
    50%
  4. D
    100%

Topic Flashcards

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Question

What is the genotype of a parent who is a "heterozygous carrier" of an autosomal recessive disorder like cystic fibrosis?

Answer

Cc (one normal allele 'C', one disease allele 'c'). They are phenotypically normal but can pass on the disease allele.

Question

In a cross between two heterozygous parents (Cc x Cc), what is the probability that an offspring will inherit the genotype 'cc' and be affected by the disorder?

Answer

25%. The Punnett square genotypic ratio is 1 CC : 2 Cc : 1 cc.

Question

True or False: In an autosomal recessive disorder, an individual must have two copies of the recessive allele to show the disease phenotype.

Answer

True. A single dominant allele (C) is enough for a normal phenotype. Only the homozygous recessive (cc) genotype is affected.

Question

What percentage of offspring from two heterozygous parents are expected to be phenotypically normal (unaffected)?

Answer

75%. This includes both homozygous normal (CC, 25%) and heterozygous carrier (Cc, 50%) genotypes.

Question

If a child of two heterozygous parents is unaffected, what is the probability that this child is a carrier?

Answer

2/3 (or about 66.7%). Among the unaffected offspring (CC and Cc), 2 out of 3 are carriers (Cc).

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