UNDERSTANDING PHENYLKETONURIA (PKU)

Phenylketonuria PKU is a rare hereditary disease. It impacts the individual's power to break down an amino acid called phenylalanine. Frequently, the liver creates an enzyme called phenylalanine hydroxylase, which transforms phenylalanine into tyrosine. In people who have PKU, this enzyme lacks function properly. As read more a result, phenylalanin