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

🧬 What is the Fragile X premutation—and why does it matter? In just 90 seconds, this animated video breaks down how a small change in the FMR1 gene can affect individuals and families across generations. 🎥 Learn about FXTAS, FXPOI, other premutation-associated conditions, and why early awareness is so important. 📲 Watch now and share to help others understand this often-overlooked part of the Fragile X spectrum. https://fragilex.org/resources/webinars/what-is-fragile-x-premutation-90-second-v

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

They are DIFFERENT. Fragile X Syndrome is often mistaken for Autism, but they are NOT the same. Fragile X Syndrome is one of the leading inherited causes of intellectual Disability and the only known single gene cause of Autism. Both conditions can involve social challenges and developmental delays, but Fragile X Syndrome has a specific genetic cause and presents with its own unique set of symptoms. Autism is a behavioural condition and has no blood test to confirm it, whilst Fragile X Syndrome