Fragile X Syndrome
Fragile X Syndrome is a genetic condition that causes intellectual disabilities and affects how the brain develops. It is caused by a mutation in the FMR1 gene on the X chromosome, which leads to challenges in learning, behavior, and social interactions. Individuals with Fragile X may experience anxiety, ADHD, and sensory sensitivities. The severity of symptoms can vary; some people may need more support than others. Early intervention with therapies can help improve communication and social skills, enhancing quality of life for affected individuals and their families.
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Fragile X syndrome is a genetic disorder caused by a mutation in the FMR1 gene on the X chromosome. It often leads to developmental delays, learning disabilities, and social challenges, particularly in boys. People with Fragile X may exhibit features such as anxiety, hyperactivity, and difficulty with communication. Physical traits can include a longer face and larger ears. The condition is inherited, meaning it can run in families. While there is no cure, early intervention and support can help manage symptoms and improve quality of life.