Fragile X syndrome is the most common cause of inherited mental retardation. The condition affects approximately 1 in 3,600 males and 1 in 6,000 females.
Fragile X syndrome causes a range of symptoms. Abilities range from mild learning disabilities to severe mental retardation. Behavioral characteristics include autism, hyperactivity, short attention span and poor eye contact.
Physical features, such as a long face, large or prominent ears, flat feet and enlarged testes, are usually more noticeable in young adults than in children, and in males more than females.
Fragile X syndrome is caused by a change in the fragile X mental retardation (FMR1) gene. The FMR1 gene is located on the X chromosome. This abnormal gene, which can be passed from generation to generation, is usually inherited through the gene that is carried by women.
A fragile X carrier is someone who has an altered FMR1 gene, but does not show any obvious signs or symptoms of fragile X syndrome. Women who are fragile X carriers have up to a 50 percent chance of having a child with fragile X syndrome. Men who are fragile X carriers will pass the altered gene to all of their daughters but none of their sons. Daughters of carrier men are expected to be intellectually normal but are at risk of having children affected with fragile X syndrome.
The genetics of fragile X syndrome are complicated. Genetic counseling is recommended when someone has a family history of fragile X syndrome or is shown to be a carrier of fragile X.
Anyone can be a carrier of fragile X syndrome. It is found among all ethnic backgrounds and racial groups. Approximately 1 in 250 women in the general population are carriers of the abnormal gene that causes fragile X syndrome. A woman of any age can have a child with fragile X syndrome, whether or not she has had previous children.
You are at greater risk if you have:
The fragile X carrier test provides specific information about whether or not individuals are fragile X carriers, and about their risks of having a child with fragile X syndrome. The test is performed on a small sample of blood. Results are usually available within two weeks. Testing provides accurate results more than 99 percent of the time. Other causes of mental retardation are not identified through this test.
There are four possible results from a fragile X carrier test:
Genetic counseling is recommended and available when someone is shown to be a carrier of fragile X.
For more information about fragile X syndrome, genetic counseling, or to arrange carrier testing, please contact the Prenatal Diagnostic Center.
Reviewed by health care specialists at UCSF Medical Center.
This information is for educational purposes only and is not intended to replace the advice of your doctor or health care provider. We encourage you to discuss with your doctor any questions or concerns you may have.
Prenatal Diagnostic Center
350 Parnassus Ave., Suite 810
San Francisco, CA 94117
Phone: (415) 476-4080
Fax: (415) 353-4077