Information about Fragile X
Fragile X Syndrome is the most common known inherited cause of learning disabilities, affecting around 1 in 4000 males and 1 in 8000 females. It can cause a wide range of difficulties with learning, as well as social, language, attentional, emotional, and behavioral problems. In addition, approximately 1 in 250 females and 1 in 600 males are carriers of the Fragile X pre-mutation. Some carriers may develop symptoms, including Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS), Fragile X Primary Ovarian Insufficiency (FXPOI) or Fragile X Premutation Associated Conditions (FXPAC). Therefore, Fragile X consists of a family of genetic conditions.
One of the aims of the Fragile X Society is to provide support to families affected by Fragile X, through providing information about the conditions. Therefore, we have a broad range of information available to you. The links below will direct you to some of the main areas.