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Advisor(s)
Abstract(s)
In phenylketonuria (PKU), weaning is considered more challenging when compared to feeding healthy infants. The primary aim of weaning is to gradually replace natural protein from breast milk or standard infant formula with solids containing equivalent phenylalanine (Phe). In addition, a Phe-free second stage L-amino acid supplement is usually recommended from around 6 months to replace Phe-free infant formula. Our aim was to assess different weaning approaches used by health professionals across Europe.
Description
Keywords
Phe-free infant formula Phenylalanine Phenylketonuria Weaning Infant; HDE PED
Citation
Mol Genet Metab Rep. 2019;18:39-44