Skip to main content

National Society for Phenylketonuria (NSPKU)

Phenylketonuria (PKU) is a rare inherited condition in which there is a build up of phenylalanine in the body. Phenylalanine is a natural substance; it is a building block of protein. PKU is looked for in all newborns in the United Kingdom by measuring phenylalanine levels in the heel-prick blood test. All babies should have this test as it allows treatment to start early in life.

The National Society for Phenylketonuria (NSPKU) offers help and support for people with phenylketonuria, their families and carers.

Who to contact

Telephone
Helpline: 030 3040 1090
Email
info@nspku.org
Website
The National Society for Phenylketonuria

Disclaimer

This information has been collected from third party providers therefore the Slough Family Information Service website and Slough Borough Council cannot accept responsibility for the accuracy of this information and recommends that parents, carers, young people, residents and professionals check with providers regarding DBS (Disclosure & Barring Service) and OFSTED registrations and CQC registrations