The Turner Syndrome Research Registry is a database specifically dedicated to Turner syndrome research. It is the only registry that allows the information stored there to be shared with many research teams for years to come.

Joining this research registry allows you to have a direct impact on research and the improvement of care for all those touched by Turner syndrome.

Turner Syndrome Global Alliance is pleased to endorse this valuable tool provided by the Turner Syndrome Society.

Click the “Learn More” button for complete details and to register.