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introduction of down syndrome
introduction of down syndrome
introduction of down syndrome
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Down’s Syndrome is named after John Langdon Down, a British doctor who first studied and described the mental disorder. He discovered the disorder in Surrey, England while working at an asylum for children with mental retardation. He called people with this disorder Mongoloids because of the physical similarities of citizens from Mongolia compared to those affected by Down’s Syndrome. Later, the term “Mongoloid” was dropped and named after John Down when Jerome Lejeune, a French geneticist who tested children with these similar physical characteristics of Mongolians, found that 97% of those tested had an extra chromosome-21, with a total of 47 chromosomes. Down’s Syndrome is a common disorder due to an extra chromosome number; it is the most common cause of mental retardation that occurs in 1 in 1,000 babies in the United States. (Genetic Science Learning Center) There are three types of Down’s Syndrome: Trisomy 21, Translocation, and Mosaicism. Trisomy 21 is the most common type of Down’s Syndrome; it occurs in 95 percent of Down’s Syndrome cases. Trisomy 21 is a disorder in which a newborn receives an extra third chromosome-21, instead of the normal 2. The second type of Down’s Syndrome is Translocation; it occurs when only a small piece of the chromosome-21 is found on another chromosome. Only 3 percent of those with Down’s Syndrome suffer from Translocation. Mosaicism is the third type of Down’s Syndrome and also the rarest; it is a disorder in which newborns have a mix of cells in the chromosome-47 that contains an extra chromosome-21. Only 2 percent of people with Down’s Syndrome possess Mosaicism. (Hauser-Cram, 15) Causes of Down’s Syndrome are still unknown. There is no way to prevent the occurrence of Down’s Syndrome,... ... middle of paper ... ...://learn.genetics.utah.edu/content/disorders/whataregd/down/> Hauser-Cram, Penny. Children with Disabilities: a longitudinal study of child development and parent well-being. Boston: Blackwell, 2001. Kumin, Libby. Classroom Language Skills for Children with Down Syndrome: A Guide for Parents and Teachers. 1st ed. Maryland: Woodbine House, 2001. Leshin, Dr Len. Down Syndrome: Health Issues. May 2009. McGuire, Dennis. Mental Wellness in Adults with Down Syndrome: A Guide to Emotional and Behavioral Strengths and Challenges. 1st ed. Maryland: Woodbine House, 2006. Skallerup, Susan, ed. Babies with Down Syndrome. 3rd ed. Boston: Woodbine House, 2008. Skotko, Brian. Fasten Your Seatbeat: A crash course on Down Syndrome for brothers and sisters. 1st ed. Maryland: Woodbine House, 2009.
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
When someone has three chromosomes in chromosome 21, it means you have Down syndrome. I know that the gene mutation in the picture is Down syndrome because when you have three chromosomes present, people tend to use the term "trisomy," which is also known as Down syndrome. Down syndrome a genetic disorder that affects not only the child or person with it, but also everyone else. Down syndrome is a mental and physical genetic disorder that is very rough on someone.
The type of mutation that occurs in Down syndrome is aneuploidy that is the irregular number of chromosomes in a cell. The most common of the three is the trisomy 21 that occurs in about 90% of people with the disorder. In this factor the human is given three copies of the chromosome 21 instead of the common two copies. This occurs due to the complications of the cell division in the process of the egg or sperm. The next case is mosaic which happen when there are inequality of cells with three copies of chromosome 21 and others with the original two copies. Mosaic appears when there is an unexpected cell division after fertilization. The last and the rarest form is translocation and that happens while the chromosome 21 in cell division is broken off and attached to another chromosome. Since the disorder is unexpected there are numerous amounts of risk factors that are possible based on the severity of the person.
In 1866 British doctor John Langdon Down defined and described the characteristic symptoms of Down Syndrome but was unsure of the cause. It wasn't until 1959 that Dr. Lejeunne and his team in Paris showed that people with Down Syndrome have an additional chromosome. We normally have 23 pairs of chromosomes, each made up of genes. The cells of people with Down Syndrome include three chromosome #21 instead of two. The extra 21st chromosome causes an extra dose of proteins. These proteins cause the typical features of Down Syndrome. While the fetus with Down Syndrome is developing, its body cells do not reproduce as fast as usual. That is the main reason why these babies are smaller than average after birth and their brain not as big as those of other newborn children.
Down's syndrome is not a disease and therefore people with Down syndrome do not suffer nor are they victims of their condition.Down Syndrome is a natural disorder coming from a chromosome defect. It is a genetic condition in which a person has 47 chromosomes instead of the usual 46. Which causes mental impairment and physical deformity.For example short stature , broad facial profile and weak muscle tone.It occurs in approximately one in every 800 live births.It is the most frequently occurring chromosomal disorder. Down syndrome is not related to race, nationality, religion or socioeconomic status.(medline plus)
The three types are Trisomy 21, translocation and mosaicism. Trisomy 21 is also known as nondisjunction. Usually a person has two separate copies of chromosome 21. In nondisjunction, the
Down syndrome is caused by a problem with a baby’s chromosome. Chromosomes are cell structures made up genetic DNA (“Chromosomes”). Most people with Down syndrome have 47 chromosomes. This changes the way the brain
I’m writing my paper on Down syndrome. Down syndrome is also known as trisomy 21. This happens when a person has a full or partial extra copy of chromosome 21. Most individuals with Down syndrome are small stature, have low muscle tone, and have upward slanted eyes. In America babies born with Down syndrome occurs one in every six hundred and ninety-one births. There is approximately four hundred thousand American’s that have Down syndrome and approximately six thousand babies born a year with this condition.
Down syndrome, a genetic disorder, is the most common cause for intellectual disabilities, occurring at an average of one out of every 700 births (CDS, 2006). This disorder is caused by the extra chromosome 21 (also known as Trisomy 21). According to Hassold and Sherman (2002), the probability of giving birth to a child with DS is not linked to any race, ethnicity, socioeconomic status or geographic location. Maternal age seems to be the only etiological factor that may cause DS.
Chromosomes are genetic material that is present in every cell of all living things. They are responsible for cell functions, which eventually lead to body functions. Lejeune made an astonishing discovery in 1959 using advanced scientific techniques. He revealed that people with Down syndrome have an extra copy of chromosome twenty-one, which makes a total of forty-seven chromosomes. Scientists today are faced with the question: What causes this abnormality? Without Jérôme’s discovery, we would not be able to make advances in science with this disorder. Therefore, his discovery still affects our world today.
Trisomy 21 or more commonly known as down syndrome is a condition in which an individual has a full or partial extra copy of chromosome 21 (What is Down Syndrome?, 2012). It was first described as a disorder in 1866 by doctor John Langdon Down and it is the most common cause of cognitive impairment (Heyn, 2014). Today there are three known types of down syndrome trisomy 21 or called nondisjunction, translocation, and mosaicism. Regardless of the type of down syndrome a child may have, they all have an extra portion of chromosome 21 present and the cause is still unknown today (What is Down Syndrome?, 2012). With the cause unknown many people have misconceptions or don’t understand what down syndrome is. That is why I chose to research down
Down syndrome can be caused by a random error in cell division which results in a presence of an extra copy of chromosome 21. This type of error is called nondisjunction. Usually when one cell divides in two, pairs of chromosomes are split so that one of the pair goes to one cell, and the other from the pair goes to the other cell. In nondisjunction something happens that makes both chromosomes from one pair go into one cell and no chromosome from that pair goes into the other cell. A lot of the time, the error occurs at random during the formation of an egg or sperm. After a lot of research is has been discovered that in more than 90% of cases, the extra copy of chromosome 21 comes from the mother in the
What causes Down syndrome? Robertsonian translocation occurs when part of chromosome 21 breaks off during cell division and attaches to another chromosome (usually chromosome 14) (Crosta). There are 46 chromosomes in the body. 23 are from the mother and 23 are from the father. When there is another copy or a half copies of chromosome 21, you will have a child with Down syndrome. The most common type of Down syndrome is Trisomy 21. It is where the body has 47 Chromosomes instead of 46 (Crosta). Trisomy 21 is caused by a problem in the cell division called non-disjunction; it leaves a sperm or an egg cell with an extra copy of chromosome 21. 95% of Down syndro...
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.
Down syndrome can be caused for three different reasons. The most prevalent reason is called trisomy 21. This means that rather than having 46 chromosomes you have 47. This is the cause for approximately ninety- five percent of the people affected by Down syndrome. The extra chromosome is usually found on the twenty-first pair. The next cause only affects 1 percent of the Downs population. It is known as mosaicism. This is caused from an error during cell division right after conception has occurred. It has been seen that with mosaicism some of the cells have 47 chromosomes while other cells only have 46 chromosomes. The last reason can be traced back to the parent's. It is known as translocation. The twenty-first chromosome is translocated on to another chromosome. The parents could be carrying the chromosome that translocates. This form of Down syndrome affects only 3-4 percent of the people living with Downs.