Fragile X syndrome is the most common form of inherited developmental disability. A problem with a specific gene causes the disease. Normally, the gene makes a protein you need for brain development. But the problem causes a person to make little or none of the protein. This causes 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:
- Fragile X Syndrome (National Library of Medicine)Fragile X syndrome is the most common form of inherited developmental disability. A problem with a specific gene causes ...
- Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. Usually, males ...
- Fragile X syndrome is a genetic condition involving changes in a gene on the X chromosome. It is the ... Fragile X syndrome is caused by a change in a gene called FMR1 . A small part of the gene ...
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- Other Fragile X Syndrome FAQs (Eunice Kennedy Shriver National Institute of Child Health and Human Development)Find answers to other common questions about Fragile X syndrome, such as conditions associated with Fragile X syndrome, how it is inherited, and how the genetic mutation occurs.
- About Fragile X Syndrome (Centers for Disease Control and Prevention)Learn more about fragile X syndrome, symptoms, testing, treatment, early Intervention and support
- Fragile X Syndrome (Eunice Kennedy Shriver National Institute of Child Health and Human Development)The genetic disorder Fragile X syndrome, which results from mutations in a gene on the X chromosome, is the most commonly inherited form of developmental ...
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