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What is Dyslexia?These are some signs of dyslexia Thanks to the interest from the National Institutes of Health and the research they have supported, we now have more information on what causes reading difficulties than ever before. The International Dyslexia Association and National Institutes of Health adopted this definition of dyslexia in 2002. A New Research Definition of Dyslexia: Research into the genetics of dyslexia is ongoing. Dyslexia is an inherited condition. Researchers have determined that a gene on chromosome #6 is responsible for dyslexia. Several other genes have been identified as probable causes of dyslexia. This is an exciting area of research and new studies are investigating the genetic links to dyslexia. If one parent has dyslexia, the probability of a child also having dyslexia is 50%. Dyslexia results from a neurological difference. The right hemisphere of dyslexic individuals is larger and neurons are found in areas of the brain that are not typical of individuals without dyslexia. Research is ongoing into this neuronal migration. Dr. Sally Shaywitz, one of the NIH researchers, has discovered that people
with dyslexia actually use different parts of the brain when performing phonemic
tasks or reading than people without dyslexia. Using functional Magnetic Resonance
Imaging her team has discovered what happens in the brain of dyslexics and more
efficient readers. In addition, her research has shown how to actually rewire
the brain of dyslexics to look like that of an efficient reader. (See Effective
Teaching.) |
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