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Ethical issues of genetic testing
Ethical issues of genetic testing
Ethical issues of genetic testing
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Prenatal genetic testing is being performed constantly somewhere. Prenatal genetic testing is an ethical issue itself, but the advice these parents are given is a much larger ethical issue. Is it just to preform prenatal testing; in other words is it fair and are the risks and benefits provided equally to the parents? Are parents treated fairly when making the decision for prenatal genetic testing? “As tests become part of routine clinical practice, they become normalized and harder to question or decline” (Deans, Hill, & Lewis 2013). Parents are pressured into preforming these tests because they do not want to feel as if they are being judged or making the wrong decision according to someone else. Prenatal genetic testing can be as simple …show more content…
This is not the case for all parents though. Some will see things such as defects or abnormalities that they did not want to see or even imagine their precious child having. That then leads to the question of options for the pregnancy. Abortion is another huge ethical topic that could be related back to prenatal genetic testing. The concern is what the physicians or medical personnel are advising these parents to do with the pregnancy once they see an abnormality. Medical personnel have a huge impact on the decision these parents will make for their child. Parents trust medical personnel to tell them the truth and guide them in the correct direction with what is best for them and their unborn child. There are hundreds of opinions on weighing the risks and benefits of keeping or terminating a pregnancy. The term ethical pops up all over the internet when you search for prenatal genetic testing because of the pregnancy termination. “In January of 2007, the American College of Obstetrics and Gynecology (ACOG) released new guidelines recommending that all pregnant women, not just women over 35, be offered prenatal “fetal chromosomal screening” and, if warranted by the screening, prenatal diagnostic testing” (Mills & Erzikova,
A person's individuality begins at conception and develops throughout life. These natural developments can now be changed through genetically engineering a human embryo. Through this process, gender, eye and hair color, height, medical disorders, and many more qualities can be changed. I believe genetically engineering a human embryo is corrupt because it is morally unacceptable, violates the child's rights, and creates an even more divided society.
In today’s modern age science is moving at a rapid pace; one of those scientific fields that has taken the largest leaps is that of genetics. When genetics first comes to mind, many of us think of it as a type of science fiction, or a mystical dream. Yet genetics is here, it is real, and has numerous ethical implications.
In Laura Purdy’s account of Genetics and Reproductive Risks: Can Having Children Be Immoral?, Purdy’s claim is that conception of a child is immoral when there is reasonable concern of a genetic disorder and if prenatal screening is not done to see how likely it is for your child to obtain that disease, then it is wrong. Purdy thinks it is immoral to reproduce when we are at high risk of transmitting a disease or defect and she says it is wrong to reproduce without knowing the consequences of our genome. The birth of a child at risk of a serious defect could be prevented by abortion or preventing conception of a child. And conception is only allowable once a person has undergone a prenatal screening and if a selective abortion would be done, and for those who are against abortion must be extremely careful not to conceive.
Over 40 years ago, two men by the names of James Watson and Francis Crick discovered deoxyribonucleic acid, or DNA. DNA is hereditary material in humans and almost all other organisms (What is DNA?). From this finding, gene therapy evolved. Today, researchers are able to isolate certain specific genes, repair them, and use them to help cure diseases such as cystic fibrosis and hemophilia. However, as great as this sounds, there are numerous ethical and scientific issues that will arise because of religion and safety.
The history of harmful eugenic practices, spurring from the Nazi implementations of discrimination towards biologically inferior people has given eugenics a negative stigma (1,Kitcher, 190). Genetic testing, as Kitcher sees it through a minimalistic perspective, should be restrained to aiding future children with extremely low qualities of life (2,Kitcher, 190). He believes that genetic engineering should only be used to avoid disease and illness serving the role of creating a healthier human race. He promotes laissez-faire eugenics, a “hands off” concept that corresponds to three components of eugenic practice, discrimination, coercion and division of traits. It holds the underlying works of genetic testing, accurate information, open access, and freedom of choice. Laissez-faire eugenics promises to enhance reproductive freedom preventing early child death due to genetic disease (3,Kitcher, 198). However there are dangers in Laissez-faire that Kitcher wants to avoid. The first is the historical tendency of population control, eugenics can go from avoiding suffering, to catering to a set of social values that will cause the practice of genetics to become prejudiced, insensitive and superficial. The second is that prenatal testing will become limited to the upper class, leaving the lower class with fewer options, creating biologically driven social barriers. Furthermore the decay of disability support systems due to prenatal testing can lead to an increased pressure to eliminate those unfit for society (4,Kitcher, 214).
There are several types of genetic tests that can give us a broad amount of information about ourselves, our parents and/or children (What is testing?). Personally, I see advantages and disadvantages to it. Anyone is able to find the probability of them having a disorder or disease and start dealing with before it gets to a lethal stage. For women, it is reassuring to know whether a disorder that they possess can be passed on to their children or not. They can also know whether their child is healthy or not before it is even born. It also impacts on how scientists deal with diseases since they are given a different output of the disease at its early stages and allows them to study it until a cure is found. But what happens when your private information goes public? People will be treated differently because of a high risk of having a cancer in the future. In your CV, your past experiences and your qualities will be accompanied by your genetics test results that inform the company whether you will be a risk to them in the future. A new kind of discrimination will be created in our society. A second major disadvantage to genetic testing is people using it for “superficial” purposes like changing children’s eye colors and other biological characteristics that should not be changes. Above the disadvantages are the benefits which are why I am all for the genetic testing for health-related purposes.
If two parents get tested and find out that their child could have the disease, they could choose to get an abortion, which would be abusing the benefits of genetic testing. In the Jewish testing article it says “or they may choose to end the pregnancy” (Goldschmidt). In this case, taking the life of an unborn child due to genetic testing is an example of how genetic testing can be morally unsound. Also, if a cure is found for genetic testing, the treatments can be very harsh. In the Patients in Limbo article is says “every month for the first two years of her life” (Marcus). Although a cure was found, this child had to undergo extreme treatment in order to have the chance of being cured for the condition. As just a young child, depending on the type of treatment it is, this can be too extreme for such a young patient and can deteriorate the young ones body. In this situation, although genetic testing led to results, it also led to things that can cause pain and suffering, which is not what genetic testing should be used to
Kolata, Gina. "Ethics Questions Arise as Genetic Testing of Embryos Increases." The New York Times. The New York Times, 03 Feb. 2014. Web. 18 Mar. 2014.
The Human Genome Project is the largest scientific endeavor undertaken since the Manhattan Project, and, as with the Manhattan Project, the completion of the Human Genome Project has brought to surface many moral and ethical issues concerning the use of the knowledge gained from the project. Although genetic tests for certain diseases have been available for 15 years (Ridley, 1999), the completion of the Human Genome Project will certainly lead to an exponential increase in the number of genetic tests available. Therefore, before genetic testing becomes a routine part of a visit to a doctor's office, the two main questions at the heart of the controversy surrounding genetic testing must be addressed: When should genetic testing be used? And who should have access to the results of genetic tests? As I intend to show, genetic tests should only be used for treatable diseases, and individuals should have the freedom to decide who has access to their test results.
In recent years, genetic testing has become a popular topic in the media. Usually involving cheek swabs, blood samples, or amniotic fluid samples, the procedure is relatively simple and can help diagnose genetic disorders, determine ideal medication types, or simply determine the patient’s heritage. It has saved many lives from cancer and other afflictions, but to say that genetic testing is always the correct choice is false. There are many issues with the tests, considering that they are new to the medical world. Genetic testing is mostly harmful because of privacy concerns, how underdeveloped it is, and the risk of it pushing a mother to abort her child.
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.
In today’s world, people are learning a great deal in the rapidly growing and developing fields of science and technology. Almost each day, an individual can see or hear about new discoveries and advances in these fields of study. One science that is rapidly progressing is genetic testing; a valuable science that promotes prevention efforts for genetically susceptible people and provides new strategies for disease management. Unnaturally, and morally wrong, genetic testing is a controversial science that manipulates human ethics. Although genetic testing has enormous advantages, the uncertainties of genetic testing will depreciate our quality of life, and thereby result in psychological burden, discrimination, and abortion.
There are variables that could affect her choice. She could be poor, the child could have a birth defect, and so on. Giving her a right to decide whether she should abort the baby, it’s entirely her choice. What if the mother was raped or she got pregnant from incest? Would you traumatise this mother with the child of the rapist for 9 months, and would you allow an inbred child that will most likely have a disability and be put through literal hell?
In such positions, the resolution to terminate a pregnancy may be argued as the most ethical choice. The mother is also considered to have a reasonable level of ethical responsibility to the fetus, because she did not take enough precautions to ensure avoid conception (Cline, 2014). The mother’s ethical responsibility to the fetus may not be enough to deprive her of choice of abortion; it may be enough to ascertain when an abortion can be ethically selected (Cline, 2014). When a woman does not wish to carry an abortion to term, it will be unethical for law or any other person to force them to do so.... ...
First of all, I want to start by saying that I 'm not discriminating the disabled community, but this is a very large number that could possibly be diminished with the help of genetic testing. (1) I believe that there is nothing wrong with testing the genes of an unborn child to possibly determine if it could develop a genetic disorder in the future. One of the advantages that genetic testing provides is that the parents could now be informed of the situation, and keep track of their unborn child 's health. I 'm sure those parents are pleased with this technology, and the chances to be able to keep track of their baby. This a baby, and is something very precious, and valuable, and I believe that parents want to keep track of anything that may happen with the unborn child. I 'm sure that a large amount of people would agree would agree that they don 't want to suddenly take the hard hit. When the news is presented in the delivery room. This serves more as an advantage than a disadvantage, due to the fact parents. Pull be more prepared, or possibly have the option to abort it. This is a right that the parents should have regardless of the opposing side arguments towards it. Im a hundred percent sure that the opposing side has very strong arguments towards genetics testing, and one of the main ones is "playing God." The opposing side believed that some things in