The National Fragile X Foundation supports and researches about the Fragile X condition. Fragile X is a family of genetic conditions, which can impact individuals and families in various ways.
These are related in that they are all caused by gene changes in the same gene, called the FMR1 gene. The Fragile X includes: the Fragile X syndrome, the Fragile X-associated tremor/ataxia syndrome, and the fragile X-associated primary ovarian insufficiency. The National Fragile X Foundation unites the Fragile X community to enrich lives through educational and emotional support. They also seek to promote public and professional awareness, and advance research toward improved treatments and a cure for this condition. At the left and right hand sides of the homepage you will find several categories that provide more information about this condition, and about the labor of this foundation in the society. Some of these categories are For the Newly Diagnosed, What is Fragile X, Cause, Characteristics, Testing, Medical, Education, Carriers, and many more. 
