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Early Feeding Practices in Infants with Phenylketonuria Across Europe

2018-09Journal article Open access
http://hdl.handle.net/10400.17/3049
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Authors

Pinto, A
Adams, S
Ahring, K
Allen, H
Almeida, MF
Garcia-Arenas, D
Arslan, N
Assoun, M
Atik Altınok, Y
Barrio-Carreras, D

Advisor(s)

Abstract(s)

In infants with phenylketonuria (PKU), dietary management is based on lowering and titrating phenylalanine (Phe) intake from breast milk or standard infant formula in combination with a Phe-free infant formula in order to maintain blood Phe levels within target range. Professionals use different methods to feed infants with PKU and our survey aimed to document practices across Europe.

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Keywords

Breastfeeding Inherited Metabolic Disorders PKU, Phenylketonuria Phe, Phenylalanine Phe-Free Infant Formula Phenylalanine Phenylketonuria Infant Practices HDE PED

URI

http://hdl.handle.net/10400.17/3049

Citation

Mol Genet Metab Rep. 2018 Aug 8;16:82-89

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Publisher

Elsevier

DOI

10.1016/j.ymgmr.2018.07.008

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PED - Artigos

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