Family and friends of Jude Hudson have raised £10,000 for The Schinzel-Giedion Syndrome (SGS) Foundation in July Emma Hudson, Secretary […]

SGS Family Conference August 12-14th 2022 If you didn’t make our Family Conference, you can catch up on all the […]

The Schinzel-Giedion Syndrome Foundation is Appointing New Trustees The mission of The Schinzel-Giedion Syndrome Foundation is to provide support to […]

https://www.newswise.com/articles/grant-helps-uah-s-baudry-lab-research-protein-s-interactions-in-so-called-orphan-diseases

The Schinzel-Giedion Syndrome Foundation is a member of COMBINEDBrain In January 2020 The Schinzel-Giedion Syndrome Foundation joined COMBINEDBrain, a non-profit […]

Read about Nuala and Ophelia at Rare Disease UK Nuala’s Story Share this article and raise awareness of Schinzel-Giedion Syndrome. […]