Participate in Research to Accelerate Discoveries in SGS

In this photo: Xavier

SGS Natural History Study

The SGS Global Patient Registry is a secure platform where families share health information about their child. By enrolling in the SGS Patient Registry and completing the registry surveys on a yearly basis, parents help transform this information into a Natural History Study, enabling researchers to track disease progression, identify patterns, and support the development of future treatments.

Watch the video to learn about the SGS Natural History Study and how you can participate

SGS Biorepository

The SGS Biorepository collects de-identified blood samples from children with Schinzel-Giedion syndrome and their families to support vital research and improve future care. Participation is currently open to U.S.-based families, with international expansion underway.

Watch the video to learn how you can participate and help advance research for children with SGS
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