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MedlinePlus: Phenylketonuria

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Description: Definition, causes, symptoms and treatment.
Phenylketonuria: MedlinePlus Medical Encyclopedia Phenylketonuria (PKU) is a rare condition in which a baby is born without the ability to properly break down an amino acid called phenylalanine. Phenylketonuria (PKU) is inherited, which means it is passed down through families. Both parents must pass on the defective gene in order for a baby to have the condition. This is called an autosomal recessive trait.
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Page title:Phenylketonuria: MedlinePlus Medical Encyclopedia
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