The Turner Syndrome Global Alliance was founded in 2011 by a group of parents, patients, and clinicians who believed that people with Turner syndrome deserved more — more research, more specialized care, and more community. Fifteen years later, that belief has grown into a global movement.

We have helped build a network of 80+ specialized clinics, funded over $2.4 million in research, launched the InsighTS Registry, and connected thousands of families with the care and community they need.