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A couple, each phenotypically normal, have a child with phenylketonuria, an autosomal recessive trait - VCE - SSCE Biology - Question 6 - 2012 - Paper 1

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A couple, each phenotypically normal, have a child with phenylketonuria, an autosomal recessive trait. The chance that their second child will have the trait is: A.... show full transcript

Worked Solution & Example Answer:A couple, each phenotypically normal, have a child with phenylketonuria, an autosomal recessive trait - VCE - SSCE Biology - Question 6 - 2012 - Paper 1

Step 1

Determine the genetic background

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Answer

Phenylketonuria (PKU) is an autosomal recessive condition. This means that both parents must be carriers of the recessive allele (represented as 'a') for a child to express the trait (aa). If both parents are phenotypically normal (AA or Aa), they can either be homozygous dominant (AA) or heterozygous (Aa).

Step 2

Analyze the parent's genotype

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Answer

Since the couple has a child with PKU, both parents must be carriers (Aa). We can illustrate their genotypes:

  • Father: Aa
  • Mother: Aa

This means their potential offspring could result from the following combinations: AA, Aa, Aa, aa.

Step 3

Calculate the probability for the second child

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The offspring distribution shows that there is one in four (1/4 chance) for a child to be homozygous recessive (aa), which indicates that the child will have phenylketonuria. The question specifically asks for the chance that their second child will have the trait, which remains independent of the first child's condition.

Step 4

Conclusion

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Answer

Thus, the chance that their second child will inherit phenylketonuria is:

A. one in four.

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