Pros And Cons Of Genetic Testing

Many medical advances are being made today in the area of genetics. One of the most talked about is prenatal genetic testing. The purpose of prenatal genetic testing is to obtain information on a baby's health before they are born. This new technology will definitely improve the quality of human life. Diseases will be diminished and through new advances some diseases might even be eliminated. Children will be at less risk to have major health problems in their lives adding positively to their life experience. Prenatal genetic testing will also affects society as a whole.

What are the most serious genetic diseases and what are the pros and cons of genetic testing?

Genetic testing has brought about many changes in the way many couples look at conceiving and raising families. Through genetic testing you are able to screen for the increased chance that a fetus may have one of many congenital disorders, or even identify gene changes that are responsible for a disease that has already been diagnosed (Genetic Testing, March 2015). Unfortunately genetic testing is not always exact, in some cases giving parents false negatives or false positive results. Even if the results are accurate, there is the burden of knowledge once you know the results indicate a genetic abnormality such as Down’s syndrome. While caring for a 2 year old male patient with developmental delays and anotia, I learned that genetic testing had been started but never completed on the child. Genetic testing could help to identify genetic disorders that led to the child’s developmental delays and possible future disorders that may develop. The ethical dilemma I will be discussing to the ANA Ethical dilemma of the impact of informed consent of genetic testing on children for adult onset diseases and disorders.

There are two main ways genetic testing places a constraint on a child’s right to an open future. The first of these is that the revelation of a child’s disease status can change his life narrative and the way parents and others treat him, and substantially alter his or her life’s trajectory (Davis _____). Parents may feel guilty or shelter their not-yet-sick

Genetics has become a very important topic of discussion in the healthcare field. There are more and more diseases being linked to certain genes in the DNA. Carrier: Untangling the danger in my DNA, by Bonnie J. Rough, is one example of the modern problems people have to deal with in regards to genetics and genetic testing. The author writes about the problems she faced. She had some very difficult decisions about her possible offspring as well as herself. Rough writes about her struggle with deciding if she should get a genetic test for a gene that causes a disease that has been passed on through her families for generations. The reader also learns about her and her husband’s experience of getting pregnant and the steps they took to try

Genetic testing has become a highly controversial issue among both the general population and the scientific community. It is a process that exposes a person’s entire genome sequence, allowing it to be read and evaluated to identify potential risks for genetic diseases or diseases that could be passed onto offspring (Holt Productions, 2012). With thousands of genetic tests already being used, and more being established, it seems logical to put this growing technology to use. Some agree that it is a person’s right to know and understand his or her genetic makeup. However, others argue that, despite the benefits of genetic testing, caution should be used to carefully inspect the risks associated with this new technology.

<br>4. The rights of knowing someone's own health status and keeping that information private to oneself should be provided to all members of a society. Only the individual should have full access to information about his own genetic constitution and others should be prevented by legal regulations. As we have said above, the results of genetic tests can sometimes be detrimental to the individual. If a person does not want to know the information, its nobody's business nor right to declare it. This includes even not explaining favorable test results without the individual's request.

If the genetic information is only accessible to the individual then there is a decreased chance of such discrimination occurring because the information is disclosed to who the individual wishes to. Genetic information can raise questions about personal responsibility, personal choice versus genetic determinism, and concepts of health and disease. Personal factors, family values, and community and cultural beliefs can mould the reactions to these issues. For example the response to the genetic information and suggestion from physicians after the test will be drastically different in a society where traditions and religion determine life choices, such as India, than to a more individually liberal society like the USA. Even in a progressive society that has had specific ethnic groups for multiple generations disparities with medical technology are common. A study conducted, using the national representative data, in the USA with the sample that consisted of 1724 men and women of non-Hispanic whites, Latinos, and African American background. Results exposed significant differences by racial/ethnic groups in knowledge and concerns about the potential misuse of genetic testing. Significantly higher levels of mistrust in a physician and the medical system was a common thread within minorities. The genetic tests can be a way of ridding anxiety attached to the assumed inheritance of genetic disease due to family background whilst for others the genetic test reveals their reality. The results can have a great deal of a psychological impact upon the individual. The possibility of developing a genetic disease alone can create anxiety within some. The psychological impact from the results revealed is another issue that society is concerned about. A

In recent years genetic modification has been advancing. Genetic modification is when a living organism has been altered to a specific state of characteristics. So far scientist has made one attempt to modify genes from an embryo recently. Whether they were successful or not is question unanswered yet. Gene modification can be great and all. However, is it right to modify genes? Apparently, the population agrees to modify genes since there has been licenses of approval for gene modification. If Society cared about gene modification, then there would be signs of disapproval of gene modification. However, this is viewed morally wrong in my point of view. The pros of modifying genes are that defeating diseases, potential to live longer, genetic diseases, and able to select character traits of babies. The cons of modifying genes are failures on the way to perfecting genetic modification, genetic modification babies can have more greater problems, very expensive, and when does it stop?

There is much controversy around the issue of genetic testing. These controversial issues range from being "unnatural" or against god 's will. There are several different ways to tests genetics but they all have one thing in common: they test for changes or mutations in chromosomes, genes, and proteins. These tests can provide answers for many families who want to know whether their children have become inflicted with a condition due to their family 's genetics, the health of the mother during the gestational period, or by some strange twist of the unknown. Despite all of the controversy, Genetic Testing is acceptable for determining whether an unborn child is at risk of developing a debilitating and/or deadly condition, relieving the worry of parents, and preemptively treating any condition that the child may have.

Although the gene chip will enable an individual to know whether he/she has a genetic disease, that person may not want to know the information. Many people are frightened that a positive finding on a genetic test will result in discrimination and ostracism because the society will consider them abnormal (Easthope 2005). The other concern is that with genetic test information one might lose or might be unable to get a job or insurance. There have been concerns that with the knowledge of one’s medical information after a gene test, he/she might suffer a psychological problem especially when the results reveal that one suffers from a terminal disease or has high possibility of suffering from one (Willis 2009).

Genetic genealogy can set the stage for discrimination and inequality for those seeking minority status, for benefits and government handouts, or alternately, it can hold individuals back because of racism or bigotry; and lead to ‘genetically repackaged discrimination’. There is an uneven playing field, with some entities recognizing genetic testing results, yet others are rejecting it. While seeking personal identity is a worthwhile endeavor, another perspective brings a host of psychological, social, legal, political, and ethical worries. It is possible to uncover undesirable, or unexpected genetic ancestral ties that could lead to diverse identity issues, and other emotional, or financial consequences. Increasingly, genetic testing, or DNA, is used as a genealogical resource; it has potential to be used as a tool by narrowing down possibilities, but it can, also, be scientifically inaccurate. There are limitations in the science, both with interpretation of tests results, and with the databases. Avoiding inaccuracies requires sampling strategies and creating human population margins from genetic data. In addition, interpretation of ancestry tracing needs to be made less complicated for the consumer. While uncertainties are inherent, geneticists are optimistic about the future of genealogy using DNA.

Genetic information can be identified at any point throughout a person’s lifespan from pre-conception until after death. In addition to heritable, biological information, family history, genetic test results, and medical records are also sources of genetic information” (Jenkins & Lea, 2005). We are put in a position to gather and retain information that could be utilized for a better future, but is confidentiality involved for the sake of profiting? Ask yourself, who should have access to genetic information? Who owns and controls it? How can families resolve conflicts when some members want to be tested for a genetic disorder and others do not?

On July 27th, 1997, my life and my family’s lives changed. My mother received a phone call from my pediatrician, letting her know that her three-year-old daughter had a positive result for cystic fibrosis (CF). When she describes that moment in her life, she says that it was the most stressful time she can remember. As a pharmacist, she had always known what CF was but she had no idea how to raise a child who had been diagnosed with it. To ease her mind my pediatrician referred her to a genetic counselor (GC). I was three when I was sitting across from a genetic counselor, so I never knew what the role of a genetic counselor was or any specifics of the profession. When I was in high school my mom mentioned her visit to a genetic counselor and I asked her to expand on that

provide an early treatment that would permit a person to live longer and more meaningful and