Fragile X syndrome (patient information)
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| Fragile X syndrome (patient information) | |
 | |
|---|---|
| Location of FMR1 gene | |
| ICD-10 | Q99.2 |
| ICD-9 | 759.83 |
| OMIM | 309550 |
| DiseasesDB | 4973 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Assistant Editor-in-Chief: Alexandra M. Palmer
Overview
Fragile X syndrome, also called Martin-Bell syndrome or Marker X syndrome, is a genetic condition involving changes in part of the X chromosome. It is the most common form of inherited mental retardation in males and a significant cause of mental retardation in females.
What are the symptoms of Fragile X syndrome?
- Mental retardation
- Large testicles (macro-orchidism) after the beginning of puberty
- Large body size
- Tendency to avoid eye contact
- Hyperactive behavior
- Large forehead or ears with a prominent jaw
Family members who have fewer repeats in the FMR1 gene may not have mental retardation, but may have other problems. Women with less severe changes may have premature menopause or difficulty becoming pregnant. Both men and women may have problems with tremors and poor coordination.
What are the causes of Fragile X syndrome?
Fragile X syndrome is caused by a change in the FMR1 gene. The gene's code is repeated on a fragile area of the X chromosome. The more repeats, the more likely there is to be a problem.
Normally, the FMR1 gene makes a protein you need for your brain to grow properly. A defect in this gene makes your body produce too little of the protein, or none at all.
Boys and girls can both be affected, but because boys have only one X chromosome, a single fragile X is likely to affect them more severely. You can have Fragile X syndrome even if your parents do not have it.
Who is at highest risk?
Since Fragile X syndrome can be inherited, anyone with a family history of the disease is at risk.
How to know you have Fragile X syndrome?
The person will have a family history of Fragile X syndrome (especially a male relative).
There are very few outward signs of Fragile X syndrome in babies. Babies may have a large head circumference. Measurement of oversized testes in males who have reached puberty may also suggest the diagnosis. An experienced geneticist may note subtle differences in facial characteristics. Mental retardation is the hallmark of this condition and, in females, this may be the only sign of the problem.
A specific genetic test called polymerase chain reaction (PCR) is used to diagnose this disease. This test looks for an expanded mutation (called a triplet repeat) in the FMR1 gene.
In the past, a specific type of chromosome analysis was done. Such testing may still be available.
When to seek urgent medical care
Call your health care provider if you suspect the possibility of Fragile X syndrome in a child with mental retardation.
Treatment options
There is no specific treatment for Fragile X syndrome. Instead, effort is directed toward training and education so that affected children can function at as high a level as is possible. Because the condition is not rare, specific educational approaches have been developed and tested.
Diseases with similar symptoms
Where to find medical care for Fragile X syndrome
Directions to Hospitals Treating Fragile X syndrome
Prevention of Fragile X syndrome
Genetic counseling may help prospective parents with a family history of Fragile X syndrome. Genetic testing can help determine the level of risk in such a family. Accurate diagnosis is important because of the possibility of other family members inheriting either Fragile X syndrome or other problems related to an increased number of repeats in FMR1.
What to expect (Outlook/Prognosis)
The outcome depends on the extent of mental retardation.