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2 min read

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.

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