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Down syndrome is a set of cognitive and physical symptoms that result from having an extra chromosome 21 or an extra piece of that chromosome This 2014 revision takes into account extensive input from the down syndrome community, including researchers, constituency organizations, and individuals with down syndrome and their families It is the most common chromosomal cause of mild to moderate intellectual disabilities
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People with down syndrome are at risk for several other health conditions. Executive summary significant progress has been made in research on down syndrome since the first national institutes of health (nih) research plan on down syndrome was published in october 2007 The symptoms of down syndrome vary from person to person, and people with down syndrome may have different problems at different times of their lives.
Down syndrome is caused by a random error in cell division that results in the presence of an extra copy of chromosome 21.
There is no single, standard treatment for down syndrome Treatments are based on each individual’s physical and intellectual needs, as well as his or her personal strengths and limitations 1 people with down syndrome can receive proper care while living at home and in the community A child with down syndrome likely will receive care from a team of health professionals, including, but not.
Children with down syndrome are at an increased risk for some health problems, but not all will have serious health problems. Down syndrome is the most frequent chromosomal cause of mild to moderate intellectual disability. Health care providers can check for down syndrome during pregnancy or after a child is born There are two types of tests for down syndrome during pregnancy
This test can show an increased likelihood that a fetus has down syndrome, but it cannot determine whether down syndrome is definitely present
If a screening test shows an increased likelihood, a diagnostic. Down syndrome describes a set of cognitive and physical symptoms that result from an extra copy or part of a copy of chromosome 21.
