Answer:
The correct answer would be option C. 50%
Step-by-step explanation:
Phenylketonuria is an autosomal recessive genetic disorder. Phenylketonuria occurs if a person has two recessive alleles (p) for for PAH (phenylalanine hydroxylase) gene.
If the person has the heterozygous condition (Pp) for PAH gene, than he will be considered as a carrier for the disorder but if he has two dominant alleles (PP) of the disorder, he will be normal.
The child of parents, one with phenylketonuria (pp) and other who is carrier (Pp) is most likely to have 50% chances to having phenylketonuria.