Fragile X Syndrome
[fra-jɘl \- ‘eks-\ sin-drōm]
Fragile X syndrome is one of the most common inherited causes of intellectual disability, which means this condition limits a person’s ability to learn at an expected level, and function in daily life . Fragile X syndrome is caused by a change in the genetic material that mostly affects brain cells. This change makes it hard for cells to produce a protein that is needed for normal brain function. Currently, there is no cure for fragile X syndrome. The sooner children are diagnosed with fragile X syndrome, the sooner they can benefit from care and services. There are behavioral treatments, medicines, and educational services that may help.
- The average age at diagnosis for fragile X syndrome is 35 to 37 months for boys and 42 months for girls.
- Learning disabilities, behavioral problems, developmental delays, and seizures are some possible symptoms of fragile X.
- Fragile X syndrome can be an underlying cause of autism spectrum disorder.
- Females with fragile X syndrome often have milder symptoms than males.
- If you’re concerned about your child’s development, talk to your child’s doctor.
- If your child has developmental or intellectual disability with no known cause, consider asking your doctor for the fragile X syndrome test, which is called the “FMR1 DNA Test for Fragile X.”
- Currently, there is no cure for fragile X syndrome, but there are behavioral treatments, medicines, and educational services that may help your child.
- Having a diagnosis of fragile X syndrome for your child can help you connect with support groups of other families in the same situation.
- Tremors and early menopause are symptoms of disorders that can be related to fragile X syndrome. If you or other members of your family have these symptoms, discuss them with your doctor, even if you don’t have a family history of fragile X syndrome.