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Fragile X Syndrome Research Paper

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The genetic disorder I will be researching and writing on is the Fragile-X Syndrome. Fragile-X Syndrome is one of the most commonly known and inherited types of neonatal genetic disorders and mental retardations. Among the name fragile-x syndrome, it is also known by a few other names. For example, a couple of the other known names are: FXS, FRAXA, and Martin-Bell Syndrome. FXS greatly impacts areas of the brain. The disease does not directly affect the brain as a whole, but renders the body incapable of producing enough of a specific protein vital for the development of the brain. Fragile-X syndrome is existent when there is a mutation in the FMR1 gene. The FMR1 gene is essential for cognitive development as well as female reproductive function. The syndrome is caused …show more content…
Fragile-x syndrome can not be described as either recessive or dominant. Usually an affected male will be mentally retarded though as for a female who is heterozygous has a thirty-three percent chance of expressing those cognitive disabilities. There are a various amount of symptoms that are both physically manifested, and symptoms that are mental and less easy to recognize. It can be noted that those with the disability will show aggression, self-harm, impulsivity, and hyperactivity. Repetition of both words and movements is as very common symptom of those with FXS. Those are a few of the behavioral signs and symptoms of Fragile-x. As far as developmental issues go, those with the issue are more easily seen in children. They will experience and express learning disabilities on top of speech delays and problems. On more physical terms, one with the disease may have flaccid muscles, long faces, double joints, large ears, lazy eyes, prominent jaws, etc. There are many signs and symptoms of the syndrome. Although, along with many other syndromes and diseases, there are no

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