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The National Society for Phenylketonuria (NSPKU)

NSPKU is the only UK charity dedicated to improving the lives of people living with the rare condition PKU. Our goal is to support individuals and families living with Phenylketonuria across the UK.

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DHPR Deficiency

Maternal PKU, Pregnancy in Women with PKU

Version
Download 383
File Size 119 KB
File Count 1
Create Date 04/02/2020
Last Updated 25/06/2020

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Description

Maternal PKU women pregnancy phenylalanine advice preconception

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For more information use our Contact page or helpline: 030 3040 1090

For PKU Unplanned Pregnancy Emergency Advice please contact your local centre.

You can also use our documents library to access lots of important information

THE NATIONAL SOCIETY FOR PHENYLKETONURIA (UNITED KINGDOM) LIMITED is a charity
registered with the Charity Commission (Company No. 01256124 Charity No. 273670 )

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