Question

phenylketonuria is a genetic change is.... cells
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Answer 1

Phenylketonuria is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. Untreated, PKU can lead to intellectual disability, seizures, behavioral problems, and mental disorders. It may also result in a musty smell and lighter skin.

Answer 2

Answer-

Phenylketonuria  can be defined as a rare metabolic disorder caused by a deficiency in the production of the hepatic (liver) enzyme phenylalanine hydroxylase.From medical genetics, the disease phenylketonuria is inherited as a recessive phenotype and is ascribed to a causative allele that generally can be called k. Phenylketonuriais a disorder of the conversion of the amino acid phenylalanine  into tyrosine.