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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

PKU: European Guidelines – What do they mean for adults?

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Download 148

File Size 171 KB

File Count 1

Create Date 04/02/2020

Last Updated 27/06/2020

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Description

NHD article magazine Suzanne Ford 2017 key European guidelines adults issue 123

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Diagnosis, Treatment

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vast Updated 27/06/2020

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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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