Testing genetic alteration before and after birth
NURS 5315 Advanced Pathophysiology Assignment Papers.
NURS 5315 Advanced Pathophysiology
Genetics Paper – Fall 2018
DUE: October 24,
Purpose: To provide an opportunity to explore the genetic transmission and resulting pathophysiology of a specific disease/disorder of interest to the Advanced Practice Nurse student.
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). 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. The paper should reflect your synthesis and understanding of the information. References should be dated within the previous 5 years. NURS 5315 Advanced Pathophysiology Assignment Papers.
The paper must be submitted via Blackboard. Papers not submitted via Blackboard will not be graded. Specific instructions for how/where to submit are provided separately in the Course Assignments folder. Papers submitted after the due date of October 24 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. NURS 5315 Advanced Pathophysiology Assignment Papers.
Guidelines/Grading Criteria
- 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)
- 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)NURS 5315 Advanced Pathophysiology Assignment Papers.
- Describe how the genetic alteration is diagnosed and tested before and following birth. (10 pts)
- List 3 specific teaching points to provide a patient/family regarding the genetics of the disease/alteration. May include genetic transmission, counseling, specific resources available, life expectancy, etc. Does not include manifestations, therapy, treatment options. (15 pts)
- Present information in a scholarly manner (clear, grammatically correct) and reflect synthesis of information from sources. Use APA format for headings, citations and references. Conforms to 3 page length. (15 pts) NURS 5315 Advanced Pathophysiology Assignment Papers.
Testing genetic alteration before and after birth
The debate over genetic alteration is one that has been raging for years. Some believe that we should be testing and altering genes before birth, while others believe that this is an ethical slippery slope. In this blog post, we will explore both sides of the argument. We will discuss the pros and cons of testing and altering genes before and after birth. We will also touch on the ethical considerations of such a practice.
Why test for genetic alteration?
There are many reasons why someone might want to test for genetic alteration. For example, they may be concerned about the possibility of their child being born with a genetic disorder, or they may want to know if they are carrying a gene that could be passed on to their children.
testing can also provide information about a person’s risk of developing certain diseases, such as cancer. In some cases, testing can even help guide treatment decisions.
How is genetic alteration tested?
There are a few ways to test for genetic alteration, but the most common is through a blood test. This can be done before or after birth, but it is generally recommended that it be done as early as possible so that any necessary treatment can be started as soon as possible. Other tests, such as skin or hair samples, can also be used to test for genetic alteration.
What are the risks of genetic alteration?
There are many potential risks associated with genetic alteration, both before and after birth. These risks can be broadly divided into three main categories: physical risks, mental/emotional risks, and social risks.
Physical risks include the possibility of developing physical abnormalities or diseases as a result of the genetic alteration. Mental/emotional risks include the possibility of experiencing negative psychological effects, such as anxiety or depression, as a result of the alteration. Social risks include the possibility of experiencing discrimination or exclusion from social groups as a result of the alteration.
It is important to note that these risks are only potentialities; not all individuals who undergo genetic alteration will experience all or any of these risks. However, it is important to be aware of them so that informed decisions can be made about whether or not to proceed with genetic alteration.
What are the benefits of genetic alteration?
There are many potential benefits of genetic alteration. For example, parents may choose to alter the genes of their child in order to prevent them from developing certain diseases or conditions. Additionally, parents may elect to change the genes of their child in order to improve their overall physical appearance or athletic ability. Finally, parents may also use genetic alteration in order to increase the intelligence of their child. While there are many potential benefits of genetic alteration, it is important to note that this technology is still relatively new and uncertain. As such, it is important to speak with a qualified medical professional before making any decisions about altering the genes of your child.
Conclusion
Testing for genetic alterations before and after birth can help identify potential health problems early on, allowing for earlier intervention and treatment. While there are some risks associated with genetic testing, the benefits outweigh the risks for many people. If you’re considering genetic testing for yourself or your child, talk to your doctor to learn more about the risks and benefits.
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