What is Fragile X Syndrome?
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Fragile X syndrome is the most common form of inherited mental retardation. A problem with a specific gene causes the disease. Normally, the gene makes a protein you need for brain development. But the mutation causes a person to make little or none of the protein, which results in the symptoms of Fragile X.
People with only a small change in the gene might not show any signs of Fragile X. People with bigger changes can have severe symptoms. These might include
- Intelligence problems, ranging from learning disabilities to severe mental retardation
- Social and emotional problems, such as aggression in boys or shyness in girls
- Speech and language problems, especially in boys
Fragile X has no cure. You can treat some symptoms with educational, behavioral or physical therapy, and with medicines. Getting treatment early for Fragile X can help.
National Institute of Child Health and Human Development
Related Fragile X Syndrome Images and Links
Fragile X syndrome - PubMed Health - National Center for ... Causes, incidence, and risk factors. 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 ... Read MoreFragile X Syndrome - NICHD - The Eunice Kennedy Shriver National ... Fragile X syndrome is the most common form of inherited intellectual and developmental disabilities (IDDs). Fragile X happens when there is a change, or ... Read More
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Fragile X syndrome: MedlinePlus Medical Encyclopedia 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 ... Read More
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Fragile X Syndrome