Down Syndrome Of Chromosome 21 Essay

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Chromosome 21 normally contains only two copies (a Pair) of chromosomes, as do the rest of the 22 pairs of chromosomes which make up a total of 23 pairs of chromosomes (46 in each cell,) chromosome 21 is the smallest human autosome, it contains 48 million nucleotides, the nucleotides are the building material of DND, and makes up between 1.5 and 2 percent of the total DNA in cells. When each cells in the human body contains three copies of chromosome 21, known as trisomy 21, it results in a medical condition known as “Down Syndrome,” this is a chromosomal condition which affects several characteristics visual in an infant, these include: intellectual disability, facial appearance, and weak muscle tone.

Down syndrome can also happen during
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There can also be a missing segment of the chromosome in each cell, this condition will be known as “partial monosomy 21,” and another condition where a structure forms as a circle which is called Chromosome 21 Ring, or r21, Ring 21, and Ring 21, Chromosome, this is a rare condition where the chromosome 21 has a breakage at both ends and the chromosome arms join at the ends forming a circle. There is usually a loss of genetic material when this happens which may result in numerous symptoms depending on the amount of genetic materials that have been lost. In cases where very a little amount of genetic materials that have been lost there may be no symptoms of this disorder while the person is an infant, however, in the case where there is a significant loss of genetic materials the symptoms may include: mental retardation and other abnormalities which are visible in the face and eyes of the infant, there could also be abnormalities which are not visible such as abnormalities of the skeleton (sometimes visible) and internal