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Welcome to the first Klinefelter’s Syndrome Awareness Day – brought to you by the Klinefelter’s Syndrome Association (KSA).
It is 80 years since Harry Klinefelter identified the syndrome which we now know is caused by an extra X chromosome in males but 75% of those affected are still never diagnosed.
KS/XXY isn’t rare….but it is rarely diagnosed. Please help us change this by watching and sharing our great video by Jim (AJ) Howard, one of our trustees and his puppets.
Your opportunity to have your voice heard. The KSA is providing options to help you to have your say about this extremely important review. Please click here for further information.
Raising Psychologists’ Awareness of KS/XXY. Dr. Jenny Retzler, whom many of you may have met at KSA conferences, has had an article accepted by The Psychologist. It highlights the difficulties faced by many of those affected by KS/XXY and the
This year’s conference focus will be on practical and positive day-to-day support. We have worked towards having three strand running concurrently, so whether you are an individual with KS / XXY, a partner or parent or carer, supporting a friend/family
Can You Afford to Miss the KSA Conference 2025? Where can you benefit from 4 whole hours of informal chat with the leading KS/XXY experts in the country? Where can you hear KS/XXY clinic updates (or, if you prefer, chat
Research on quality of life with KS/XXY My name is Brien Mehmet, and I am a PhD student at City, St George’s University of London. Many of you will have met me at recent KSA Conferences. I am collaborating with
Vital research on KS/XXY in the justice system. Please help! The KSA are working with two forensic psychologists to look at why some KS/XXY people get involved in the justice system. The psychologists have recruited one of their MSc students, Harry Evans, to carry