An accurate and safe DNA testing to check if you are a carrier of Fragile X Syndrome (FXS) and understand if you have a higher chance to have a child with that condition.
What is FXS?
FXS (Fragile X Syndrome) is a genetic disorder characterized by mild-to-moderate intellectual disability. It is more affected in males, however, females may also be affected by the condition but usually to a lesser extent. There is no cure for this disorder and early intervention is recommended so that there is an opportunity for developing a full range of skills.
What causes FXS?
FXS is caused by a mutation in the FMR1 (fragile X mental retardation 1) gene which is located on the X chromosome. The protein made by the FMR1 gene has a role in the development of the brain (connections between neurons). When there is an expansion of the CGG triplet repeat within the FMR1 gene, it may results in learning disabilities and cognitive impairment. This abnormal gene, which can be passed from generation to generation, is usually inherited through the gene that is carried by women.
How is fragile X syndrome inherited?
A fragile X carrier is someone who has an altered FMR1 gene, but does not display or show any obvious symptoms of FXS. Women who are fragile X carriers have up to a 50% chance of having a child with FXS. Men who are fragile X carriers will pass the altered gene to all of their daughters but none of their sons. Daughters of carrier men are expected to be intellectually normal but are at risk of having children affected with fragile X syndrome.
About 1 in 800 male
About 1 in 260 female
Expanded Carrier Screening适合对象：
- Would like to understand their risk of having a child with FXS.
- Have a family history of FXS.
- Have a family history of mental retardation, developmental delay or autism of unknown cause.
- Have infertility problems associated with elevated follicle stimulating hormone (FSH) levels or premature ovarian failure (POF).
- Have a family history of adult onset ataxia and/or tremors.
- 计划怀孕的夫妻/ 已怀孕的夫妻
FXS carrier testing determine the number of CGG repeats on the X chromosome, allows for more accurate assessment of risk for premutation carriers as well as their risk of having affected children.
Why Choose GGA FXS Carrier Testing?