In this video, we’ll explore Fragile X Syndrome, one of the most common inherited neurodevelopmental disorders affecting both males and females. We’ll explain how a mutation in the FMR1 gene leads to symptoms ranging from intellectual delays and learning difficulties to behavioral challenges. We’ll also discuss the characteristic symptoms of Fragile X Syndrome, how it’s diagnosed, and the available treatments that can help improve quality of life for those affected. This video is beneficial for anyone looking to gain a deeper understanding of this syndrome, including students, medical professionals, and families of individuals with Fragile X.

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