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Down Syndrome Genetics is the study of heredity and how the traits from the parents are passed on to their offspring. There are so many human genetic disorders which are caused by problems within the gene. "A gene is the basic unit of heredity" (Tocci 25). A genetic disorder can be caused by a mutation possibly damaging the gene and affecting a single nucleotide. Down Syndrome is one out of the many genetic disorders worldwide. Around 250,000 families have a child with Down Syndrome in America (Tocci). Each year in the United States around 5,500 babies are born with Down Syndrome, and millions of people have Down Syndrome worldwide. Down Syndrome is a genetic disease where the chromosome 21 has an extra copy causing many problems making it …show more content…
Some of the children were more severe and their capability levels varied (Hine; Down Syndrome). Their main similarity was their physical features. Most of them had a flat broad face, round cheeks, brown straight hair,slanted eyes, a wrinkled forehead, a small nose, large lips and tongue, abnormally shaped ears, a yellowish skin, slightly overweight, and had a smaller head and hands (Tocci). Many of the features can be noticed at a young age in children with Down Syndrome. "Because Dr. Down was the first to record the features in these children, the syndrome bears his name. Down Syndrome is an abnormal condition marked by some degree of mental retardation and certain distinct physical features" (Tocci 11). Many people with Down Syndrome have a lower muscle tone making the muscles more relaxed and hard to control. Someone with an IQ below 70 is said to have mental retardation. The lower a persons IQ is, the more mentally deficient the person. Having a IQ between 55 and 69 is mild, 40 through 54 is medium, and 25 through 39 is severe. The IQ of children with Down Syndrome is usually between 40 and 69, but some go a lot lower (Tocci). Children with this disease were treated badly for a long time because of their mental deficiency. They were said to be unable to learn, placed in institutions, separated from the rest of society, and unloved. Now many anti - …show more content…
Some special diets can help improve conditions for people with Down Syndrome. Since most people with Down syndrome have an extra chromosome 21 scientists spend a lot of time working with this chromosome. (Hine; Down Syndrome) The scientists are working on how an extra copy of chromosome 21 can cause so many changes in features (Panno; gene disorders and gene therapy). This project is the Human Genome Project, which was started in1990. This project is very difficult because humans contain around 80,000 genes and a gene is made of a chemical compound called DNA. "A genome is all the DNA in the cell of an organism (Tocci). Thus scientists involved in The Human Genome Project are trying to unravel the basic structure of all the DNA in human chromosomes" (Tocci 113) This takes a very long time but new technologies are continuing to speed up the process. In doing this, scientists hope to figure out how to cure Down Syndrome. Down Syndrome is a genetic disease where there are changes in features and an extra copy on the 21st chromosome causing various levels of trouble functioning properly
In 1990, the first great stride of genetics took place. This was called the Human Genome Project, a large-scale operation that was designed to understand the human genome (genetic structure). Since its commencement, there have been many leaps and bounds that have taken place. For certain genetic issues that we once knew nothing about, we no...
A genetic disorder is a sickness caused by one or many abnormalities or absentees in the genes or chromosomes. One interesting genetic disorder such as cancer, are found genetic but, can also be caused and affected by many by environmental factors such as being exposed to asbestos which may increase the risk of lung cancer and many other cancers. While on the other hand most disorders like Williams Syndrome are genetic and are primarily rare and only affect a limited amount of people about one in every several thousand. Because it is a genetic disorder that is estimated between 1 in 10,000 people worldwide, primarily caused by a micro-deletion on the seventh chromosome is what indicates the disorder being Williams Syndrome.
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
“About 13 of every 10,000 babies born in the United States each year is born with Down syndrome. It affects an equal number of male and female babies” (Johnson P. A. 2014). Down syndrome is a genetic disorder that found across the world, however it is more prevalent in the United States. The cause of the disorder roots to the paring of the human chromosomes. A normal human receives 23 pairs of chromosomes, each pair coming from mother and father. In Down syndrome most people affected have an abnormal cell division of the chromosome. Both parents are carriers of the There are three types of variations that includes trisomy 21, mosaic, and translocation.
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)
Children with Down Syndrome have distinct physical characteristics. They are short in stature and have a small, round face with a high flattened ...
In 1886, physician John Langdon Down was the first scientist to identify Down syndrome. Down was the administrator of a mental institute for children in Surrey, England. From his observations and work at the institute, he was able to identify a set of children who exhibited characteristics such as short nose, broad flat face, short and broad hands, which are features commonly identified with Down syndrome. He later wrote an essay entitled “Observations of the Ethnic Classification of Idiots” in which he asserts the notion that it was possible to classify different types of health conditions through race. His essay included his now famous classification of what is today known as Down syndrome, which he categorized as the Mongol...
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.
Having Down syndrome is like being born normal. I am just like you, and you are just like me. We are all born in different ways, that is the way I can describe it. I have a normal life"(Burke, C., n.d.). Where special education is concerned, one must always remember that exceptional learners are different, not less.
crease, slightly flattened facial profile, an upward slant to the eyes, small mouth, and protruding
The Human Genome Project The Human Genome Project began in the mid - 1980s as an international scientific mission to map all the genetic material (i.e. genes) in human chromosomes and ultimately build the complete set of genetic information contained within molecules of deoxyribosenucleic acid (DNA) known as the genome. The project aims to improve the methods used to prevent and cure diseases because the keys to many of the worst illnesses of our time, like cancer and diabetes, can be found in genetic variations in DNA. The Human Genome Project is international, and has involved collaborations and contributions from researchers throughout the world, all of whom have donated their results freely to the public databases. It is the largest collaborative project ever attempted in biology, involving scientists in the USA, Australia, Japan, Germany, the UK, Italy, Russia, France, the Netherlands, Canada, Israel and elsewhere. The Human Genome Project aims to: * Determine the sequence of the four bases (adenine, cytosine, thymine and guanine) throughout all the DNA in human cells; * Identify the estimated 100 000 genes formed by the bases; * Find the locations of the genes on the 23 human chromosomes; * Store all this information on databases for future research; * Consider all the ethical, legal and social issues which arise from obtaining information about the human genome.
A genetic mutation is a permanent change in the sequence of the DNA that makes up a gene. A mutation of these sorts can be caused by either inheritance from the parent or caused sometime during the life of someone. The mutation that has been inherited is called a germline mutation. Germline mutations affect virtually the entire body, and they seem to be present in every cell. A somatic mutation, or one that is caused in the DNA of a single cell sometime during the life, can be caused by an environmental factor or a wrong bonding in the DNA molecule. These cannot be passed down to the next generation of children because they occur in a specific cell as opposed to in a reproductive cell. Some mutations occur in the embryo as it is growing. These may occur during cell division, and some of the cells may or may not inherit this mutation. Some mutations are extremely rare, and others are incredibly common. Those that occur in more than one percent across a population are considered polymorphisms. Polymorphisms are considered normal variations in DNA, and they are known to cause simple changes such as variations in blood types and hair color. Although these are not typically fatal, they can influence the creation of some disorders (Lister Hill National Center for Biomedical Communications, U.S. National Library of Medicine, National Institutes of Health, Department of Health and Human Services, USA.gov, 2013).
Down syndrome is a medical condition where extra genetic material physically and mentally delays the way that a child develops (KidsHealth). Laws have been put in place to ensure that children with disabilities, including Down syndrome, are guaranteed to a free public education (National Down Syndrome Society). However, students typically at the elementary level, do not completely understand that other students with disabilities are just like them, regardless of their disability. It is more beneficial for students with down syndrome or those with other disabilities if teachers and administrators educated other students on how people with disabilities learn and function (National Down Syndrome
Human beings are born, formed and changed from one generation to the other through genetics. When a child enters the world, there is always a lot of excitement and uncertainty as which parent will the baby look like? Genes of the both parents determines the physical makeup of a child and therefore, genetics plays a very big role in human development. Genetics chromosomes are distributed equally by the parents to the child and they play a big role in the development of the child. Genes determines the development of a fetus inside its mother’s womb and outside of the mother’s womb.