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What are the genetic variations of Down syndrome?
Down syndrome is identified at birth Down syndrome is a genetic disorder in which a person is born with an extra copy of chromosome 21. There are three genetic variations that cause Down syndrome: Trisomy 21, Mosaic Trisomy 21 or Translocation Trisomy 21. There are many ways in which theses disorders affect the body.
What happens to a person with Down syndrome?
DOWN SYNDROME Down Syndrome is a congenital disorder arising from a chromosome It comes from a defect involving chromosome 21. The condition leads to impairments in both cognitive ability and physical growth that range from mild to moderate developmental disabilities.
What are the developmental stages of Down syndrome?
During the developmental stages, a child with Down syndrome will experience developmental delays in the areas of motor development, cognitive development, language development, and social and emotional development. Down syndrome is identified at birth Down syndrome is a genetic disorder in which a person is born with an extra copy of chromosome 21.
What is the thesis of the Down syndrome thesis?
Down Syndrome Thesis: When someone sees a child or an adult with Down syndrome they automatically single them out, every person in this world is different, with a disability or with out, but that doesn’t mean they need to be treated differently.
Last Update: Oct 2021
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