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Sagot :
The duration of the this low phenylketonuria diet varies according to the development and cure of phenylketonuria in a new born that is in an Infant.
What do you mean by phenylketonuria (PKU) ?
Phenylketonuria (PKU) is an inborn error of metabolism in body which generally results in decreased metabolism of the amino acid phenylalanine (C9H11NO2).
- Phenylketonuria, generally known as PKU, is a rare hereditary condition that results in an accumulation of the amino acid phenylalanine in the body.
- The phenylalanine hydroxylase (PAH) gene is altered in PKU.
- The enzyme required to degrade phenylalanine is produced in part because to this gene.
To know more about Phenylketonuria (PKU) visit
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