Profiles of the TS organisations in countries around the world.

Welcome to the Swiss association of Turner Syndrome.

These are some brief details about our association:

  • It was founded more than 30 years ago by parents
  • We have more than 100 members
  • We support families and their turner syndrome girls as well as affected women

Most important activities:

  • Annual meeting (with medical presentations and social activities)
  • International congress (this year in Mexico)
  • Support with any information

Name of contact person and website:

  • This email address is being protected from spambots. You need JavaScript enabled to view it.
  • The website contains information about Turner Syndrome and its treatment, a questionnaire from and about Turners itself and their relatives, news and an agenda.
  • Of course there is also a contact list.