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Abstract paper on effects of down syndrome
Introduction to down syndrome
Down syndrome features
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Brittany Spence Down Syndrome Down Syndrome is a genetic disorder or disease, that occurs during chromosome division, in early human life. When a persons 46 chromosomes abnormally divides crating 47 chromosomes all together. Thus creating a full or partial 3rd copy of the chromosome 21. There are three types of down syndrome, trisomy 21 which is about 95% of cases, translocation accounts for 4% of cases and mosaicism accounts for about 1% of down syndrome cases. Down syndrome is a disease in which a person presents many physical symptoms which are very easy to notice at a first glance. The symptoms of down syndrome are flat facial physiognomy, small head, short neck, protruding tongue, antrorse slanting eyes that is abnormal for the child's
Down’s syndrome is a chromosomal condition that is caused by an extra 21st chromosome as there is an error in the body’s cell division. Every human has a nucleus in every cell in the body which contains genes that are grouped along with chromosomes. The normal number of
Down syndrome is a disorder that comes with some defects, such as in the face, heart, sight, and hearing, and other health related problems. It also is the most common genetic defect, affecting many babies. Down syndrome is caused when the chromosomes are being divided during meiosis the cell keeps both copies of chromosome #21, which means the person with Down syndrome has an extra copy in every cell in their body. This is a sad genetic disorder that can change a person's life. Even though it is a devastating gene mutation, the people with Down syndrome are some of the most loving of all people.
Down Syndrome results when one of the three types of abnormal cell divisions involving chromosome 21 occur. Roger W. Harms, a medical doctor, states, “Human cells normally contain twenty-three pairs of chromosomes. One pair comes from your father and one pair comes from your mother.” In each pair, one chromosome comes from the father, and one comes from the mother. One of the three genetic variations that can cause Down Syndrome is Trisomy 21. This version of Down Syndrome occurs more than 90% of the time. It re...
Most cases of Down syndrome are not inherited. When the condition is caused by trisomy 21, the chromosomal abnormality occurs as a random event during the formation of reproductive cells in a parent. The abnormality usually occurs in egg cells, but it occasionally occurs in sperm cells. An error in cell division called nondisjunction results in a reproductive cell with an abnormal number of chromosomes. For example, an egg or sperm cell may gain an extra copy of chromosome 21. If one of these atypical reproductive cells contributes to the genetic makeup of a child, the child will have an extra chromosome 21 in each of the body's cells.
Down syndrome is a very common disorder now a day’s, but not many know what it actually is. Down syndrome was a topic that was not as common back in that day. “John Langdon Down, an English physician, published an accurate description of a person with Down syndrome. It was this scholarly
It is well known that children have Down syndrome within physical features. They are not different than a person who does not have Down syndrome, but their physical features are quite different such as, facial appearance in the face, which is flatter. They also have a slant within their eyes, smaller ears and protruding tongue which is slightly bigger and suspends out a part from the mouth. (2)
Down Syndrome is a condition that cannot be physically passed on from one person to the next. It is a genetic disorder that is inherited through our parents when something goes wrong during pregnancy. As a result, they have a combination of features typical of Down Syndrome, including some degree of cognitive disability, as well as other developmental delays. One thing we should always keep in mind is that they are children and having Down Syndrome comes second.
Down syndrome, also known as “trisomy 21” is a genetic condition in which a child is born with an extra chromosone which causes certain features and delays in development. In sexual reproduction (meiosis) the new cell will have half of the mothers chromosones 23 and half of the fathers chromosones 23 to make a total of 46 (23 pairs) in the new cell (zygote). In a child with Down Syndrome, they will have an extra chromosone 21 making a total of 47 chromosones. There is no specific reason why this extra chromosone is present, but the older the mother is when giving birth, the more likely that her baby will have Down syndrome. Down Sydrome is named after John Langdon Down, the first person to describe the condition in 1866.
It is a well known fact that all living things, humans included, are made up of cells. The nucleus of a typical cell in the human body is made up of 23 pairs of chromosomes. Half of the pairs come from each parent. In some individuals there is a full or partial extra copy of chromosome 21 present; these individuals have Down Syndrome (National Down Syndrome Society). Down Syndrome is a genetic disorder that most people know very little about. Since Down Syndrome is something that very few people know much about, this paper will include a lot of information about the disorder that is not well known to the general public. In this paper I will discuss what exactly Down Syndrome is and provide background information and history, describe how and when the disorder is diagnosed, provide insight of what life is like for a person with Down Syndrome and I will do my best to clear up many misconceptions that people often have about individuals with Down Syndrome.
Down's Syndrome Down's syndrome is a genetic condition involving an extra chromosome, this change occurs around the time of conception. A person with Down syndrome has forty-seven chromosomes instead of the usual forty-six. A relatively common genetic disorder, Down's strikes 1 out of 600 babies. In 95 percent of all cases, the disorder originates with the egg, not the sperm, and the only known risk factor is advanced maternal age-at age 35, a woman has 1 chance in 117 of having a baby with Down's; at 40, her odds are 1 in 34. Graves, 1990.
crease, slightly flattened facial profile, an upward slant to the eyes, small mouth, and protruding
Down Syndrome, or Trisomy 21, has a specific set of physical symptoms that many people are familiar with, along with a common set of cognitive symptoms. Most people, even those unfamiliar with Down Syndrome, can recognize the face of a child or adult with the chromosomal condition. This is because Down Syndrome features a face with a slightly flatted nose and eyes that slope upward. In ad...
It is caused by an extra 21st chromosome. This is also known as trisomy 21. Instead of 46 chromosomes in each cell it was determined that an extra 21st chromosome affected Down syndrome, this occurs 95% of the time. There are three copies of this chromosome. It is causes by a cell error called non-disjunction. Two other types are mosaicism and translocation. Non-disjunction causes faulty cell division and produces three copies of the 21st chromosome instead of two. Either the sperm or the egg don't separate during division causing the extra chromosome to replicate in every cell. As stated above it is responsible for 95% of Downs.
The cause of this disorder is because of an extra chromosome in the body. About 90% of Down Syndrome cases are caused by this extra chromosome, chromosome 21 (this is why it is also called Trisomy 21). An extra chromosome originates in either the sperm or the egg. When the egg and the sperm unite to form the fertilized egg, two instead of three chromosomes in chromosome 21 are present. As the cells divide the extra chromosome is repeated in every cell.
(S Aivazidis., 2017) • Down syndrome is also associated with other diseases such as: leukemia, seizures, vision problems, diabetes, dementia and Alzheimer's disease. (S Aivazidis., 2017) 3. Down Syndrome and the development Myeloid leukemia has been diagnosed mostly in infants and children. Myeloid Leukemia is a type of cancer of the blood. Myeloid leukemia has a low number of leukemic blast in the bone marrow, and mutations in GATA1 gene.