Klinefelter’s Syndrome affects 1 in 600 males but 75% are never diagnosed.
Klinefelter’s Syndrome isn’t rare…..but it is rarely diagnosed.
Please help us to change that by telling a doctor, a dentist, a nurse, a teacher, a colleague or a friend.
In-person programme KSA Conference 2023 KSA Conference and AGM Saturday 13th May 2023 8.30 – 9.00 Arrive and sign-in 9.00 – 9.10 Conference
10th May is Klinefelter’s Syndrome Awareness Day in the UK Klinefelter’s Syndrome affects 1 in 600 males but 75% are never diagnosed. Klinefelter’s Syndrome isn’t
KSA Conference 2023 The KSA are delighted to send present the draft programme and ticket information for the 2023 KSA Conference. There is a very
The KSA Annual Conference 2023 will be held at the Stuart Hotel in Derby on 13th and 14th of May with the Friday Night Get-together
Researchers at the University of Huddersfield are studying people with KS/XXY syndrome and their experiences of every-day skills like memory, paying attention, and controlling impulses.
There is currently some disruption to supplies of Tostran gel. If your pharmacy is having difficulty obtaining it, please tell them to phone the suppliers,
Through our website and helpline, we provide information and support for all affected by KS/XXY including families, medical professionals, teachers and anyone else who comes into contact with people diagnosed with KS/XXY.
National Helpline: 0300 111 47 48
Our very grateful thanks to Childline for allowing us to link extensively to their website.
© 2023 Klinefelter’s Syndrome Association Charity No: 1058319
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