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Prader-Willi syndrome

Find out about Prader-Willi syndrome (PWS), which is a rare genetic condition that causes a wide range of physical symptoms, learning difficulties and behavioural challenges.

About this information

This NHS content is written for people in England. Services, entitlements and contact routes may differ in other countries.

Find out about Prader-Willi syndrome (PWS), which is a rare genetic condition that causes a wide range of physical symptoms, learning difficulties and behavioural challenges.

Content supplied by the NHS website

Content supplied by the NHS website, refreshed 20 August 2026. View the original NHS article ↗

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