Retts Syndrome

Rett Syndrome Rett Syndrome affect about one female out of 10,000 it is a really rare neurobiological disorder of using. It was believe until latterly that it only affected females since the number of males with the syndrome it very small. The child seems to be growing and developing normally and then suddenly sugar developing and most cases losses skills and abilities. The main cause of Rett Syndrome is a change in a single gene. NICHD discovered in 1999 that the Methyl-binding protein 2 (MECP2) genes on the X chromosome is where the change generally occurs. as well a mutation on gene 4, 5 occurs amidst 90-95 percent of the time to females with the syndrome. The major function of the MECP2 gene is for teaching of the nervous system. This does not mean that every individual with the syndrome has a genetic mutation or if a person has a mutation on this particular gene they dont necessarily show usual signs of Rett syndrome. Researcher is still cartoon other genes to see if they might cause Rett syndrome. The changes usually get a line between three months and three years of age. Most rasping symptoms for children with Rett syndrome are loss of purposeful hand causa, speech, balance and coordination problems, rest problems and anxiety and social-behavioral problems. They also develop Stereotyped hand campaign a very distinctive feature of Rett syndrome it can skip from hand clapping, patting or wringing which can become almost nonstop. Individuals with Rett Syndrome very much have intellectual disability/ mental retardation. It is realistic to bouncing into your 40s and 50s with the syndrome just it a very difficult and challenging life. Majority doesnt converse or walk and the only way of colloquy is with their eyes. willing need someone to care for them since they are not fit using their movement and need to follow circumscribed diets and give-and-take for their many problems. Along with the typical syndrome ass ociated with Rett syndrome a huge of...If y! ou compulsion to get a full essay, order it on our website: OrderCustomPaper.com

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