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Fragile X is a group of conditions: Fragile X syndrome, Fragile X-associated tremor/ataxia syndrome (FXTAS), Fragile X-associated primary ovarian insufficiency (FXPOI), and more emerging premutation carrier issues we are just learning about and passed through generations, often unknowingly. https://hubs.ly/H0RyK0J0 | The National Fragile X Foundation

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

In honor of World Fragile X Day, we're re-sharing this 90 second animated video to help educate everyone about Fragile X - Fragile X syndrome, the Fragile X premutation, Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS), and Fragile X Primary Ovarian Insufficiency (FXPOI). #worldfragilexday #fragilexawareness | The National Fragile X Foundation

🧬 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