Who we are

The Fragile X Syndrome Association was founded in 1995 to cater for the needs of those families with children affected by Fragile X Syndrome, bringing together families and professionals. Fragile X Syndrome (FXS) is a genetic disorder of familiar transmission, linked to the X Chromosome. It can cause difficulties such as learning or intellectual problems.
It affects 1 in 4000 males and 1 in 6000 females, and 1 in 250 women is a carrier with no clinical symptoms.

One of the basic objectives of the Association is to provide orientation and support to families who have been diagnosed.

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Associació Catalana X Fràgil next to the families

Plaça del Nord, 14 (col·legi La Salle Gràcia) 08024 Barcelona / Tel.-Fax: 93 217 09 39 / info@xfragil.cat