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Phenylketonuria (PKU) is an inborn error of metabolism caused by the failure of the enzyme phenylalanine hydroxylase to metabolise phenylalanine, one of the amino acids. There is consequently an accumulation...
Phenylketonuria (PKU) is an inborn error of metabolism. As recently as 30-40 years ago those affected grew up severely mentally retarded and often physically handicapped. With the advent of new screening...
Phenylketonuria - PKU for short - is the commonest metabolic disorder in the UK. People with PKU cannot metabolise phenylalanine, one of the amino acids found in protein foods, and if left untreated the...
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