When you purchase a custom written paper from us you are getting a FREE plagiarism report — guaranteed! Actually, everything is not that difficult as it seems at a glance. For Matthew, it is the 22nd chromosome. Carriers can carry the translocation on to their children.
This is the rarest type, where only some cells have an extra chromosome The other comes from your father. Real life stories will make Down syndrome research papers more convincing and captivating to read. What Down Syndrome is A.
With Down syndrome, this extra chromosome leads to a range of issues that affect you both mentally and physically.
Today, I would like to talk about two different ways a child can be born with Down Syndrome, and why the difference between the two is important.
That difference is that Matthew was born with a specific kind of Down Syndrome. Let me tell you. Point 3 Tell in your Down syndrome research paper about different ways of improving the quality of life for people with this disorder. So, you are about to start writing a Down syndrome research paper. There is one important difference between gene translocations and disjunctions.
One chromosome in each pair comes from your mother. National Down Syndrome Society Website: Her 21st and 22nd chromosomes are attached, so she only technically has 45 chromosomes. People with Down syndrome tend to have certain physical features in common.
We suppose that you do not really want to go deep into genetics and write about karyotypes, meiotic nondisjunction, and so on.
Carriers of a translocation also have a higher risk of infertility and miscarriage. You have learned the difference between translocation and disjunction, and why the difference is important in the families affected by Down Syndrome, including mine.
So if something goes wrong with them, it can have far-reaching effects. This is a possible plan that you may use to prepare your Down syndrome research paper. It is not the child itself- Matthew is indistinguishable from other kids with Down Syndrome.
Common conditions include heart problems and trouble hearing and seeing. You may pay with PayPal. Down Syndrome is the most common genetic disorder- 1 in every children born in the U.
But what is it? Buy today and save your money. March 21, became the first World Down Syndrome Day. The effects of all three types are very similar, but someone with mosaic Down syndrome may not have as many signs and symptoms because fewer cells have the extra chromosome.
National Institutes of Health: Having a cousin with Down Syndrome sparked my interest, and after researching I have learned that the two most common ways people are born with Down Syndrome differ in one important way.
Some will grow up to live almost entirely on their own, while others will need more help taking care of themselves. Because she is a carrier, other people in my family are likely to be carriers as well. We get half our genetic information from our mother, and half from our father.Down syndrome - parents, teachers and students at a late stage in their professional training as doctors, health visi- tors and psychologists - to ﬁ ll in a questionnaire telling.
People with Down syndrome tend to have certain physical features in common. For example, they often have flat noses and small ears.
Their mental abilities will vary, but most have mild to moderate issues with thinking, reasoning, and understanding. View Research Paper Outline Topic: Down syndrome from BIOL at Virginia State University.
Jennetta Green Research Paper Outline Topic: Down syndrome Introduction (Background Information/History)%(8). All 3 types of Down syndrome are genetic conditions (relating to the genes), but only 1% of all cases of Down syndrome have a hereditary component (passed from parent to child through the genes).
Heredity is not a factor in trisomy 21 (nondisjunction) and mosaicism. *the abbreviation ds is for down syndrome SPECIFIC PURPOSE- to inform my audience about Down syndrome INTENDED AUDIENCE- Psychology Class THESIS- Today, I will go over the history of Down syndrome, causes, diagnosing down syndrome, and its place in society/5(1).
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