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Fragile X Syndrome Analysis

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Fragile X Syndrome Analysis
Fragile X Syndrome is a genetic mutation that causes people to have intellectual disabilities, these include delays in talking, erratic behavior, and can cause other disabilities like ADHD and autism. It can only be caused by the person's parents having an infected X chromosome, specifically the FRM1 gene. It includes a narrow face, large head, large ears, flexible joints, flat feet, and a prominent forehead, social anxiety, problems thinking, and much more.

Most babies can’t be diagnosed, until later in life. The only thing they can tell is it has a large head. If there is a risk of getting it, they will do a PMR test to see if they have it. There is no cure for it, but people with it get special education to help them. The only way to get
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