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.
• www.turner-syndrom.ch
• 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.