Nail Patella Syndrome UK
Also known as: Nps (uk)
We strive to provide support, advice and information to any person with NPS and also to work alongside the medical profession by providing documented evidence, genetic explanations and up-to-date research studies that may be taking place.
Activities & Mission
We strive to provide support, advice and information to any person with NPS and also to work alongside the medical profession by providing documented evidence, genetic explanations and up-to-date research studies that may be taking place.
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Where this charity is registered to operate, as self-declared to the Charity Commission. These are regulatory classifications, not a list of active programmes, and don't necessarily indicate fundraising activity in each location.
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Frequently asked questions about Nail Patella Syndrome UK
What does Nail Patella Syndrome UK do?
We strive to provide support, advice and information to any person with NPS and also to work alongside the medical profession by providing documented evidence, genetic explanations and up-to-date research studies that may be taking place.
When was Nail Patella Syndrome UK registered as a charity?
Nail Patella Syndrome UK was registered with the Charity Commission for England and Wales on 27 January 2003 as charity number 1095621. It has been registered for 23 years.
Who runs Nail Patella Syndrome UK?
Nail Patella Syndrome UK is governed by a board of 3 trustees. The chair of trustees is BRIAN SUGDEN. Trustees are legally responsible for the charity's governance and are listed in full on its profile.
Where does Nail Patella Syndrome UK operate?
Nail Patella Syndrome UK operates across 3 areas: Northern Ireland, Scotland and England And Wales.
Is Nail Patella Syndrome UK a registered charity?
Yes — Nail Patella Syndrome UK is a registered charity in England and Wales, charity number 1095621.
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Also Known As
- Nps (uk)
Data & trust
- Register data refreshed
- 26 October 2026
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- How metrics are calculated