NewsNUTRIENTSWednesday, May 13, 2026 · May 13, 2026
Nutritional and Therapeutic Strategies in Paediatric Phenylketonuria: A Narrative Literature Review.
WHY IT MATTERS
Recent peer-reviewed research on Phenylketonuria that may be relevant for patients and caregivers.
Phenylketonuria (PKU) is an autosomal recessive disorder characterised by an inborn error of phenylalanine (Phe) metabolism. Such errors are attributed to pathogenic gene variants causing phenylalanine hydroxylase (PAH) deficiency, impairing the hydroxylation of phenylalanine to tyrosine in the Phe ...
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