Last Updated: 8 August 2024
Phenylketonuria
Last Updated: 8 August 2024
Phenylketonuria
Phenylketonuria is a rare genetic disorder where the amino acid phenylalanine builds up in the body due to a deficiency in the enzyme phenylalanine hydroxylase. Untreated phenylketonuria can lead to intellectual disabilities, behavioural problems, and seizures. Early diagnosis and dietary management significantly improve outcomes for individuals with phenylketonuria.