Asociación Española del Síndrome de Klinefelter (XXY)
A Spanish nonprofit declared to be of public benefit, providing information, guidance, and support to people with Klinefelter syndrome (XXY) and their families throughout Spain.
About Asociación Española del Síndrome de Klinefelter (XXY)
About the association
The Asociación Española del Síndrome de Klinefelter (XXY) is a nonprofit that provides information, guidance, advice, and support to adults and families living with Klinefelter syndrome, a genetic condition affecting males who have an extra X chromosome. Spain's Official State Gazette (BOE No. 57, dated March 5, 2024) published the resolution declaring the association to be of public benefit.
Who it serves
The association focuses on people diagnosed with Klinefelter syndrome (KS/XXY), their families, and the health professionals who care for them. It works to raise awareness, promote social, educational, and workplace inclusion, and encourage research aimed at earlier diagnosis.
Support and activities
- Information and guidance about Klinefelter syndrome
- Support for adults with KS and their families
- A network of medical specialists and other professionals
- Employment and training programs, including courses
- Recreational activities such as summer camps
- Annual conferences and family gatherings
- Publications and an informational blog
Organization
The association is run entirely by volunteers and funded through member dues and donations. Its unpaid board includes President Benjamín Gómez, Vice President Nacho Hernández, and attorney Marina Soler Gómez, among others. Its medical director is Dr. Carlos Balmori Boticario.
Contact
WhatsApp: +34 692 859 333 or +34 614 708 890. Email: hola@asociacionxxy.es. The association is also on Instagram, YouTube, and WhatsApp.
Klinefelter syndrome support