Before someone is diagnosed with Fragile X syndrome, all of the signs are there, but it can take a while to see Fragile X. If your child has unexplained developmental delays, ask about a simple blood test to confirm or rule out Fragile X. Because it is a genetic disorder, knowing is important not only to your child but to past and future generations. Learn more about testing at https://hubs.ly/H0t1Bmj0. | The National Fragile X Foundation
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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
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