The Turner Syndrome Society advances knowledge, facilitates research, and provides support for all persons touched by Turner syndrome.
Staff members answer questions via phone and e-mail, work with local groups, create resources, plan events, and keep our website up to date and relevant to the needs of our unique community.
The TSSUS is recognized as a national non-profit 501 (c) (3) EIN# 41-1596910 organization providing health-related resources to patients, families, and physicians for the diagnosis and treatment of Turner syndrome.