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Phenylketonuria

GeneticPhenylalanine hydroxylase deficiency1934 (described by Asbjorn Folling)Inherited
TypeGenetic
CausePhenylalanine hydroxylase deficiency
First Known1934 (described by Asbjorn Folling)
TransmissionInherited

About Phenylketonuria

Untreated, brain-damaging levels of an amino acid build up. Folling traced it after a mother noticed an odd smell in her children. Newborn blood spot screening from the 1960s was pioneered for PKU. A special low-protein diet started early in life allows normal development.

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