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Weaning Practices in Phenylketonuria Vary Between Health Professionals in Europe

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Mol Genet Metabol Rep 2019_18_39.pdf561.58 KBAdobe PDF Download

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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.

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Phe-free infant formula Phenylalanine Phenylketonuria Weaning Infant; HDE PED

Citation

Mol Genet Metab Rep. 2019;18:39-44

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Elsevier

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