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Conclusions of down syndrome
Introduction to down syndrome
Non physcial characteristics of down syndrome
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Recommended: Conclusions of down syndrome
Down syndrome was discovered in the 1800’s by a man named John Langton Down. Down syndrome1 is a condition that occurs in the chromosomes. The syndrome affects the intellectual ability of the person effected, their facial appearance and causes hypotonia2. Children born with this usually experience different types of birth defects. These birth defects can include heart defects and intestine blockage. People with Down syndrome are also at a high risk of developing other medical conditions. Some medical conditions include gastro esophageal reflux3, celiac disease4, hypothyroidism5, and leukemia6. Also some visual and hearing problems can arise. There are three types of Down syndrome. The three types are Trisomy 21, translocation and …show more content…
Physical characteristics do not show while in the mother’s womb, but are apparent from birth. A child with Down syndrome will have flat facial features, usually with a larger forehead. They will have a smaller head with smaller ears, than the average person. Their ears might also have an odd shape to them. People with Down syndrome have shorter necks, bulging tongues, and have eyes that slant upward. Although they can have these physical features, it does not mean that they will have every single one of them. A person with Down syndrome might have a normal tongue or regularly shaped ears. An infant with Down syndrome can be born at a normal size. Although they can be born at a normal size and weight, the infant will develop twice as slow as a child without Down syndrome …show more content…
has been estimated to be over 400,000. However, this number is derived from faulty assumptions – the total population from the 2000 US census, 281.4 million people, divided by the most current frequency of live births, 691 equaling 407,236. Unfortunately, this technique takes no account of the gradual increase in frequency or the increase in lifespan of people with Down syndrome. Thus, we don’t actually know how many people with Down syndrome currently live in the U.S.4. Some estimates put the worldwide population of people with Down syndrome at more than 6 million. More research is needed to ascertain whether this number is accurate. (GDSF, 2011, para.
In John Barker’s Ancestral Lines, the author analyzes the Maisin people and their culture centered around customs passed from previous generations, as well as global issues that impact their way of living. As a result of Barker’s research, readers are able to understand how third world people can exist in an rapid increasing integrated system of globalization and relate it not only to their own society, but others like the Maisin; how a small group of indigenous people, who are accustomed to a modest regimen of labor, social exceptions, and traditions, can stand up to a hegemonic power and the changes that the world brings. During his time with these people the author was able to document many culture practices, while utilizing a variety of
d) Name the conditions the non-healthy zygotes have. Zygote 1 has monosomy (it has a missing chromosome); Zygote 2 and 3 has trisomy (they have an extra chromosome).
Marie Jean Philip was a leader, advocate, and researcher for the deaf community. Most famously known for being one of the original researchers in studying American Signe Language and Deaf Culture. She earned her respect and became an admired figure for her monumental bilingual-bicultural movement. Her influence spread throughout not only the United States, but to children and adults around the world.
The book Native Son by Richard Wright is about an African American man growing up in the south. The main character Bigger Thomas often finds himself in trouble throughout his life from the beginning to the end. The author uses his views and thoughts through Bigger about American society. Bigger worked for a rich man named Mr. Dalton and had “accidentally” murdered his daughter Mary. As a result of that a domino effect of misfortune began to happen. Bigger was later arrested and put on trial because of his actions I felt like I was watching a man sinking through quicksand and with every movement or attempt to free himself making the situation worst. He only murder because fear of getting caught in her room, a white woman’s room. Mary was drunk and the Dalton’s would have thought Bigger was trying rape her or something. It was very distressing that Mary had to die but Bigger was only doing what he thought at the time was right.
Native son by Richard wright is a novel revolving around a young African American named bigger Thomas and his life working for the Daltons family. In a situation caught between faith and death, bigger must decide what he has to do to prove his innocence or fight after being caught in the midst of a violent act.
In telophase, these separate chromatids uncoil to become chromosomes. This division produces two identical cells.
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.
There is no actual behavior or environmental factor that could cause Down syndrome. Down syndrome is mainly caused by three different disorders. Trisomy 21, Mosaic Down Syndrome, or Translocation Down Syndrome, are three different types of causes. “Trisomy 21. About 95 percent of the time, Down syndrome is caused by trisomy 21 — the child has three copies of chromosome 21 (instead of the usual two copies) in all cells. This is caused by abnormal cell division during the development of the sperm cell or the egg cell.” Trisomy is the most common cause for the Down syndrome disorder. The Mosaic Down syndrome is a one of the rare causes that the disorder has. This happens when both normal and abnormal are caused by cell division after fertilization. Translocation Down Syndrome occurs when a part of the chromosome 21 attaches itself to another chromosomes and then it has two unusual copies of the chromosome. Children who have the disorder are different individuals and have different facial appearance. “Infants with Down syndrome may be average size, but typically they grow slowly and remain shorter than other children the same age. In general, developmental milestones, such as sitting and crawling, occur at about twice the age of children without impairment.” Knowing about all the causes or symptoms in Down syndrome can help to try to figure out a way to help the
An individual who has Down syndrome can be recognized as different from others since he or she have different physical features, but the question is, what causes individuals to have deformed face, little different features than someone who does not have Down syndrome? The reason some individuals are born with Down syndrome is because of an extra chromosome, this chromosome, which carries number 21. It is also known as Trisomy 21. Having this sort of disability, does not truly affect their life in a way they are not able to live, but it affects their cognitive levels, their physical growth of the child with Down syndrome. As the mother goes for an ultra sound, doctors can detect that the child within the mother’s womb has Down syndrome. (1) Mothers over age 35 have higher risk of giving birth to a child with Down syndrome, and 1 in every 1,000 women at the age of 30. In addition, in every 100 women, who age 40 there is a mother has a child with this case. As woman ages there is a higher chance of conceiving a child with Down syndrome than a woman who is in her mid-20s or younger. (2) This essay will highlight the effects and supports of Down syndrome in children.
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 is a genetic disorder, associated with the presence of an extra chromosome. Downs is characterized by mild to severe mental impairment, weak muscle tone, shorter stature, and a flattened face. Down syndrome is not a very common disease, one in every 691 children are born with Down syndrome. The disability is an illness that people are born with and is not contagious. Most people with Downs have a life expectancy of about 40 or 50 years of age. They only live for that short amount of time because they begin to develop a similar disease to Alzheimer’s. “100% of people with Down syndrome will develop some physiologic signs of Alzheimer’s when they are over 35 years old in the U.S” (Statistics about Down Syndrome). They also die earlier because having Down syndrome increases the risk of leukemia 15-20 times in the US. Therefore most people with Downs will die because of leukemia or heart problems before the age of 50.
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.
of the cells, instead of the norm of two. Generally, Down syndrome is not hereditary since it is
During prophase I, homologous chromosomes pair and form snynapses. The paired chromosomes are called bivalents, and the formation of chiasmata caused by genetic recombination becomes apparent. The bivalent has two chromosomes and four chromatids, with one chromosome coming from each parent.
There are two main types of thalassemia. The first one is Alpha thalassemia. This occurs when a gene or genes related to the alpha globin protein are missing or mutated. It happens mostly in Southeast Asia, the Middle East, China, and in those of African descent. If one gene is missing or damaged: Your red blood cells might be smaller than normal. You will have no symptoms and you will not need treatment. If two genes are missing or damaged, you will have very mild anemia that will typically not need treatment. This is called alpha thalassemia minor or alpha thalassemia trait. If three genes are missing: You will have mild to moderately severe anemia. This is called hemoglobin H disease. If it is severe, you may need blood transfusions.