How is Fragile X syndrome inherited is a very common question and one of the first things a newly diagnosed family asks. Let’s be clear – Fragile X is an inherited condition. With a very rare exception, when the FMR1 gene is deleted, the gene mutation came from either the individual’s father or mother. However, we all don’t talk genetics every day, so it can be a hard concept to follow. In fact – surprisingly – we still hear of doctors incorrectly stating how the gene mutation is passed down. Ad

Have you participated in a clinical trial? Now is the time! Together, the FRAXA Research Foundation and the National Fragile X Foundation encourage families living with Fragile X to participate in clinical trials. We do not currently have an approved treatment for Fragile X syndrome, though there are a few under investigation. Investigational treatments go through rigorous testing, including clinical trials, and must be approved by the FDA before they are available for public use. There are seve

Fragile X Syndrome (FXS) is a rare genetic disorder that profoundly affects a person’s cognitive development, behavior, and physical health. It is the leading cause of mild-to-severe intellectual disabilities like autism spectrum disorder. Fragile X Syndrome has no cure. However, therapy and medication can help manage the symptoms. Clinical trials also continue to explore new possibilities for managing and potentially mitigating the impacts of FXS. Learn more from our blog: https://studies.scien