Fragile X syndrome
Fragile X syndrome is a genetic condition involving changes in part of the X chromosome. It is the most common form of inherited intellectual disability in boys.
Martin-Bell syndrome; Marker X syndrome
Fragile X syndrome is caused by a change in a gene called FMR1. A small part of the gene code is repeated on a fragile area of the X chromosome. The more repeats, the more likely the condition will occur.
The FMR1 gene makes a protein needed for your brain to function properly. A defect in the 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.
A family history of fragile X syndrome, developmental problems, or intellectual disability may not be present.
Behavior problems associated with fragile X syndrome include:
- Autism spectrum disorder
- Delay in crawling, walking, or twisting
- Hand clapping or hand biting
- Hyperactive or impulsive behavior
- Intellectual disability
- Speech and language delay
- Tendency to avoid eye contact
Physical signs may include:
- Flat feet
- Flexible joints and low muscle tone
- Large body size
- Large forehead or ears with a prominent jaw
- Long face
- Soft skin
Some of these problems are present at birth, while others may not develop until after puberty.
Family members who have fewer repeats in the FMR1 gene may not have intellectual disability. Women may have premature menopause or difficulty becoming pregnant. Both men and women may have problems with tremors and poor coordination.
Exams and Tests
There are very few outward signs of Fragile X syndrome in babies. Some signs may include:
- Large head circumference in babies
- Intellectual disability
- Large testicles after the start of puberty
- Subtle differences in face features
In females, excess shyness may be the only sign of the disorder.
Genetic testing can diagnose this disease.
There is no specific treatment for Fragile X syndrome. Instead, training and education have been developed to help affected children function at the highest possible level.
National Fragile X Foundation -- http://www.fragilex.org
How well the patient does depends on the amount of intellectual disability.
Complications vary depending on the type and severity of symptoms.
- Recurrent infections in children
- Seizure disorder
Fragile X syndrome can be a cause of autism or related disorders, although not all children with fragile X syndrome have these conditions.
Genetic counseling may be helpful if you have a family history of this syndrome and are planning to become pregnant.
Shapiro BK, Batshaw ML. Intellectual disability. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 19th ed. Philadelphia, PA: Saunders Elsevier; 2011:chap 33.
Reviewed By: Chad Haldeman-Englert, MD, FACMG, Wake Forest School of Medicine, Department of Pediatrics, Section on Medical Genetics, Winston-Salem, NC. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Bethanne Black, and the A.D.A.M. Editorial team.