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Essay Available:
Pages:
2 pages/β‰ˆ550 words
Sources:
Check Instructions
Style:
APA
Subject:
Health, Medicine, Nursing
Type:
Research Paper
Language:
English (U.S.)
Document:
MS Word
Date:
Total cost:
$ 11.66
Topic:

Brain Disorder: Huntington Disease

Research Paper Instructions:

General Guidelines: Select a disorder/disease state that is a result of a genetic alteration. This is a formal paper, formatted and referenced per APA guidelines. The paper should be no more than 3 pages (excluding title page and references). Content that exceeds the 3 page limit will not be graded.
Include a minimum of 3 references - the McCance & Huether text is a starting point and is NOT included in the 3 references and may not be included in citations. You may not use direct quotes. You may not reference the powerpoint slides/lecture. The paper should reflect your synthesis and understanding of the information. References should be dated within the previous 5 years.
The paper must be submitted via Canvas. Papers not submitted via canvas will not be graded. You will need to submit the paper in the Genetics Paper Submission Folder. Papers submitted after the due date will not be accepted for grading or feedback and will receive a grade of zero (unless a revised date is negotiated with the faculty due to extenuating circumstances). PLEASE NOTE: If you are repeating this course you may not resubmit a paper for which you previously received a grade.
The information below indicates the areas of content expected to be included in the paper.
Guidelines/Grading Criteria
I. State why the specific genetic disorder was chosen for the paper. **Please note that in this section use of a personal pronoun is acceptable to state why the topic was selected.** (5 pts)
II. Describe the genetic disease/disorder, including incidence/prevalence across genders and ethnic groups, and specific populations/ages at risk/affected. Include the specific gene/locus affected, patterns of transmission (e.g. parent to child; affected individual to their children), and risk of transmission each pregnancy. (20 pts)
III. Explain how the genetic defect alters normal physiology and how the genetic alteration manifests. (35 pts)
IV. Describe how the genetic alteration is diagnosed and tested before and following birth. (10 pts)
V. List 3 specific teaching points to provide a patient/family regarding the genetics of the disease/alteration (may use bullet points for this content). May include genetic transmission, counseling, specific resources available, life expectancy, etc. Does not include manifestations, therapy, treatment options. (15 pts)
VI. Present information in a scholarly manner (clear, grammatically correct) and reflect synthesis of information from sources. Includes UTA title page. Use APA format for headings, citations and references. Conforms to 3 page length. (15 pts)
P.S I want to do Huntington Disease as my genetic topic. Thank you.

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Research Paper Sample Content Preview:

Huntington Disease
Name:
Institution:
Huntington Disease
Reasons for Choosing Huntington Disease
One of the diseases that are characterized by brain disorder is Huntington disease. Huntington disease causes three critical things on diagnosed individuals, including irregular movements, emotional defects, and a decline in their thinking ability. This genetic disorder is chosen for this paper as it presents an excellent opportunity for students to study its complexity, especially on the diversification of its mutation in various geographical locations. This is because studies indicate that Huntington disease mutation origin in Africa, Europe, and Japan are different. In addition to understanding the origin of HD allele mutations, studying this disorder also presents a perfects opportunity for examining some of the risks that may be developing a new mutation.
Description of Huntington Disease
As stated earlier, Huntington disease is a form of brain disorder that is characterized by irregular movements, depression, poor concentration, and coordination, among other symptoms on adults. Children might experience the same symptoms in addition to drooling and seizure. Studies have shown that between 30 to 50% of children with the disorder experience seizure (Paulsen, et al,2014). Both the male and female posses the same risk of inheriting the Huntington disease. However, Huntington Disease (HD) disorder is more common in adults between 30 to 50 years, whose form of the disorder is mostly referred to as Adult-onset HD. The juvenile form of HD experienced on children is not common compared to the adult-onset HD. HD comes as a result of mutation of HTT gene, resulting in the disorder. Mostly frequent in Europe compared to other parts of the world, studies have shown that the disease affects five in every 100,000 individuals of European origin (Urrutia, 2019).
Manifestation of HD disorder
               As had been mentioned earlier, HD is caused by an alteration of HTT gene. HTT gene’s role is to trigger the production of the huntingtin protein, which plays a vital part in brain neurons funct...
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