10 Easiest Genetic Disorders to Research for a Paper

So what are the easiest genetic disorders to research for a paper? Insider Monkey has recently published an interesting article about this topic. If you’re pursuing medicine or most other science-related fields, it’s probably inevitable that you will one day be finding yourself searching “research paper topics genetics” to do your own paper. The study of genetics is constant and there is still much more to learn. In simplest terms, genetics is the study of genes and how they are inherited. There are a number of genetics topics of interest, and under that umbrella there’s the study of chromosomes, DNA, gene mutations and much more.

Pixabay/Public Domain

The categories of genetic disorders are monogenetic disorders, multifactorial inheritance disorders, and chromosome disorders. The ones that we have on our list are common and fall mostly on the monogenetic disorders category. These different categories explain the factors as to why genetic disorders occur, for example, monogenetic represents a mutation that affects one gene. Multiple genes mutation happens when the disorder is categorized as the multifactorial inheritance disorder, and the one that affects the chromosomes is, of course, the chromosome disorders.

Now without a further ado let’s see what Insider Monkey has investigated for us. We have picked three of the easiest genetic disorders to research for a paper.

The first one is Hemochromatosis. Does your body load too much iron? This is not just a simple metabolism malfunction, but it is a metabolism disorder called Hemochromatosis. If not treated correctly, the results of this disorder could be fatal. The second research paper is Autism Spectrum Disorder. Autism Spectrum Disorder or ASD affects multiple functions of the body. The level of this disability can affect your skills as well as socialization, and a person with this genetic disorder may have difficulties socializing with others. There is no cure, but there are treatments and services that can help improve a person with ASD. The last one for today is Marfan Syndrome. A serious aortic enlargement could be a sign of Marfan Syndrome. Marfan syndrome can be inherited but there are instances where this occurs for the first time in a family. This syndrome affects the connective tissue of the body, so it can affect a variety of different body parts. About 1 in 5,000 people have Marfan Syndrome, so it is more common than you think.

For any further useful information, read Insider Monkey’s article about 10 easiest genetic disorders to research for a paper

Related posts

Leave a Comment