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Phenylketonuria Treatment: Supplementation And Early Intervention Set The Stage For Improved Long-Term Outcomes

Phenylketonuria (PKU) is an inherited disorder that causes the level of phenylalanine (phe) to be too high in the blood. Phenylalanine comes from protein digestion. People with PKU do not have enough of an enzyme called phenylalanine hydroxylase that helps break down phe.

The mainstay of Phenylketonuria Treatment is following a lifelong phenylalanine-restricted diet. This involves limiting or avoiding foods that contain the amino acid phenylalanine like meat, poultry, fish, eggs, dairy and many other protein-rich foods.

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