Genetic Basics for Turner Syndrome Patients and Families

Presenter: Angela E. Lin, MD Saturday July 23rd 2016 July 23rd 2016 Turner Syndrome Society National Conference The Turner Syndrome Society was created in 1987 by a group of women in Minnesota for the purpose of networking and support. Today, we have over 600 members and over 100 volunteers to support and maintain our valuable programs. We are recognized as 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. There are chapters and resource groups located throughout the country. The TSSUS is operated by 3 staff members at our National Office in Houston, TX, 2 consultants, and is overseen by 11 nationwide board members. http://www.turnersyndrome.org/