All information on this site is correct to the best of our knowledge, however the KSA (UK) recommends that you verify all facts before acting upon them.  Medical treatment and advice should always be confirmed by your GP, consultant or family doctor.

Welcome to the

Klinefelter's Syndrome Association

The KSA was founded in 1990 and achieved Registered Charity status in 1996.

We have an annual Conference and AGM each September and an Activity Weekend each spring. A Members’ newsletter is published at least 3 times a year. We host a FREE international chat forum, (www.xxytalk.com) and an eXtra website which provides some free information to everyone and eXtra information for Members of the KSA.  There is also a (UK only) local rate AdviceLine.

 We offer support and information to all affected by, or having an interest in, Klinefelter’s Syndrome irrespective of age, gender, ethnic origin, religion, sexual orientation, age or ability.

Through our website and helpline we provide information which can assist employers, teachers, social workers and the medical professions amongst others.

Early diagnosis and a good understanding of the implications of the condition can greatly alleviate future problems for both the person with the condition and those with whom they have close contact. As a result the Klinefelter's Syndrome Association is working to raise the profile of the condition generally but within the medical profession in particular. 

The charity is run entirely by voluntary workers who make up a National Executive Committee (NEC). The charity is funded mainly through membership fees and donations.