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Ethics of genetic testing 2018
Newborn genetic screening summary
Ethics of genetic testing 2018
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Genetic testing, also known as screening, is a rapidly advancing new scientific field that can potentially revolutionize not only the world of medicine, but many aspects of our lives. Genetic screening is the sequencing of human DNA in order to discover genetic differences, anomalies, or mutations that may prove pathological. As genetic screening becomes more advanced and easily accessible, it presents society with difficult questions that must be asked about the boundaries of science and to what degree we are allowed to tamper with the human genome. To better understand the potential impact of genetic screening on our society, we must examine the potential benefits in comparison to the possible negative impact it may cause. With this knowledge in hand, we can examine what the future holds for this field of study and the best possible direction to take. Prenatal genetic screening in particular is a polarizing topic of discussion, more specifically, preimplantation genetic diagnosis (PGD). PGD is one of the two techniques commonly used to genetically screen embryos in vitro; it is usually done at the eight-cell stage of division. PGD is most often performed when there is the risk that one or both parents carry disease-causing mutations. It is extensively used by high-risk individuals trying to conceive babes who will be free of particular mutations. PGD can test for over 50 genetic conditions and even allows for sex selection if there are underlying gender-associated medical conditions. When the results are satisfactory, the selected embryo is implanted into the mother’s uterus. While a controversial technique, preimplantation genetic diagnosis is one example of some of the good genetic testing can do, more benefits will be furthe... ... middle of paper ... ...ould be allowed to continue but only under heavy scrutiny from regulating bodies. With the proper measures put into place, it can make this a healthier and better world for everyone Works Cited Genetics & Personalized Medicine. (2013). University of Ottawa Heart Institute. Retrieved on February 3, 2014 from: http://www.ottawaheart.ca/research_discovery/genetics-personalized-medicine.htm Coughlin, S. S. (2002). Future challenges for research on diagnostic tests: genetic tests and disease prevention. Journal of Epidemiology & Community Health, 56(5), 335-336. doi:10.1136/jech.56.5.335 Weeks, C. (2012, January 1). Health insurance and 'genetic discrimination': Are rules needed? The Globe and Mail. Retrieved on February 3, 2014 from: http://www.theglobeandmail.com/life/health-and-fitness/health-insurance-and-genetic-discrimination-are-rules-needed/article4197442/
Collier Roger, A race-based detour to personalized medicine, CMAJ. April 17, 2012 vol. 184 no. 7, p E351–E353.
Advantages of genetic testing may be helpful in determining whether or not you have a disease or are proba...
PGD has proven effective in patients who are of advanced age, have had recurrent miscarriages or repeated IVF failure and are either carriers of chromosomal diseases or have genetic history of such. PGD is used with an IVF to identify chromosomal mutations and genetic defects in embryos, where a cell from IVF is removed for genetic testing before implanting it into the uterus. This can either be performed as polar body biopsy,
Teutch, S., & Tuckson, R. Department of Health & Human Services, (2008). U.S. system of oversight of genetic testing: A response to the charge of the secretary of health and human services. Retrieved from website: http://osp.od.nih.gov/sites/default/files/SACGHS_oversight_report.pdf
The hereditary risk factors for cardiovascular disease are primarily those of which individuals are unable to control, the ones for which they are born with. These risk factors would include an individual’s sex, race, age, and genetics. One out of every five males has some form of cardiovascular disease and the same applies for females. More women than men have cardiovascular disease in this country, but this is only due to the fact that there are more women within the U.S. population (Weiss and Lonnquist, 2011). Men percentage wise are at a higher risk than women. There is a somewhat reduced probability for females to have cardiovascular disease before menopause. This is believed by medical researchers and scientists to be directly related to the natural hor...
Personalized medicine through the development of modern methods of molecular biology offers application of a suitable drug to the appropriate patient at the right time. The vision of personalized medicine has begun in 1990’s when the molecular research and knowledge about proteomic, genomics and genetic testing escalated. Since then pharmaceutical com-panies, scientists and regulators needed to meet the challenges that the vision was bringing with. Right now “The era of personalised medicine is already upon us” In this paper I am going to discuss this new way of dealing with diseases including several issues which are im-plemented in this section of medicine, these are as follow:
First, let's consider the situations in which genetic testing would be beneficial to patients. Genetic testing for diseases that are preventable or treatable could allow individuals to alter their lifestyles so as to treat the disease or reduce their risk of developing the disease. For instance, the E2 version of the APOE gene, which is found on chromosome 19, has been linked to heart disease (Ridley, 1999). Individuals who have two copies of the E2 gene are particularly sensitive to high-fat and high-cholesterol diets. Therefore, a genetic test to determine whether a person has the high-risk version of the APOE gene could inform a person of future health risks, thereby allowing the person to change his diet to help prev...
"Testing Children for Genetic Status." Ama-assn.org. American Medical Association, 1995. Web. 2 Feb. 2014. .
Prenatal genetic testing has become one of the largest and most influencial advances in clinical genetics today. "Of the over 4000 genetic traits which have been distinguished to date, more than 300 are identifiable via prenatal genetic testing" (Morris, 1993). Every year, thousands of couples are subjecting their lives to the results of prenatal tests. For some, the information may be a sigh of relief, for others a tear of terror. The psychological effects following a prenatal test can be devastating, leaving the woman with a decision which will affect the rest of her life.
The "Genetic Screening" Genetic Screening. NDSU,. Web. The Web. The Web.
Although genetic testing can benefit society in numerous ways, such as the diagnosis of vulnerabilities to inherited diseases and ancestry verification, it also has the precarious capability to become a tool in selecting a more favorable genetic makeup of an individuals and ultimately cloning humans. Genetic testing will depreciate our quality of life and may result in discrimination, invasion of privacy, and harmful gene therapy.
Genetic testing is a complex process, and the results depend both on reliable laboratory procedures and an accurate translation of results. Tests also vary in sensitivity, that is, their ability to detect mutations or to detect all patients who have or will develop the disease. Interpretation of test results are often complex even for trained physicians and other health care specialists.
Genetic testing is the process of sequencing six billion letters of a human genome to possibly discover genetic differences, such as how cells carry the same genome but at the same time look and function different. Genetic testing is also the process that can give foresight into pathological diseases such as different types of cancer.
Upon completion of the Human Genome project, and the information can be translated and understood, testing for certain genetic disorders can occur. According to the article titled “Genetics is the Future of Medicine” by Joseph D’Allegro, testing for disorders should...
While genetic testing may be a moral question in terms of preserving the unique advances homo sapiens have accomplished, it proves to be an undoubtable advantage in terms of evolutionary success and advancement. Genetic testing can be done in various forms and during various stages of human development, from an embryo to an elder. The U.S National Library of Medicine defines genetic testing as a medical test that identifies changes in chromosomes, genes or proteins. They also define the test as one with many pros and cons, requiring a complex personal decision. This distinction between both scientific and humanistic approaches to testing mirrors the divide in which testing is regarded as a positive or negative tool for the human species. Genetic