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Ethical issues for genetic testing
Negative impact on prenatal genetic testing
Ethical issues for genetic testing
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Ethical Dilemmas of Genetic Testing Genetic testing has rapidly become a major controversial topic in society. Genetic testing presents itself with many positive and negative attributions in the field of medicine, and should be thoroughly discussed before one should take a stance on it or when deciding on whether to have this test. The ethical dilemmas that arise from this test are not primarily focused on what the test entails, but are centered on the actions of the person of autonomy after receiving their results. This topic has two equally supported sides; however, an appropriate and just stance cannot be formed until all the facts and support have been reviewed. Genetic testing is a field of testing intended to gather critical information …show more content…
After the discovery of the chromosomal basis for genetic disorders, subsequent findings occurred quickly. Through a procedure known as amniocentesis, chromosomes could be extracted from amniotic fluid of a pregnant woman’s uterus and examined. In 1990, Mary-Claire King was credited with finding a strongly hereditary form of breast cancer. Similar genes to the ones found by Mary-Claire King were found to form a colorectal cancer shortly after her discovery. Genetic material carrying mutations have been found to code for diseases of dementia and specific cardiovascular diseases. This field of testing has continued to expand. As of today, any fetal anomaly whose genetic basis are known can be detected from a sample of amniotic fluid. Genetic testing began as an attempt to answer questions regarding the unknown causes of diseases expressed by the genetic makeup of the person carrying the disease. The theory was that once these questions were revealed ways to prevent, treat, or cure these genetically encoded diseases would present themselves. However, these questions have yet to be fully answered. Due to constraints in the information provided by these tests, an ethical dilemma was born. The testing fell short of its manifest destiny, and did not provide answers to treating all the disease caused by genetic makeup. Instead of giving answers on how to overcome all the genetically-borne diseases, the test can only inform participants of the inevitable – if accurate. (Nancy
Guidelines like these need to be formed into a federal law that people can pass in one way or another so that we can be protected from the various forms of discrimination that is possible with this kind of information. The public should be aware of what could happen if this kind of information could become public knowledge, and of the opportunities that the knowledge brings. There is no doubt that the information from genetic analysis is going to help a lot of people with all sorts of problems live longer and healthier lives. The only problem is that we have to keep the information in the hands of those who need it, and out of the hands of those who would use the information to profit or discriminate.
In Gattaca, the plot focuses on the ethics, the risks, and the emotional impact of genetic testing in the nearby future. The film was released in the 90s; yet in the present, the film does not give the impression of science fiction. Today, genetic testing is prevalent in many aspects of the scientific community. This paper will describe genetic testing, its purpose, diagnostic techniques that use genetic testing, relating Huntington’s disease to genetic testing, and the pros and cons of genetic testing.
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).
Lies never really save anybody from trouble. In this case, Arthur Miller’s “The Crucible” is a play following the Salem witch trials, and lies are used to sabotage. Causing havoc within the town. There are 3 big components within “The Crucible” where lies get people into more trouble than they were already in. For starters, Abigail and the girls were caught dancing in the woods, they lied, which started this whole devastation.
When it comes to genetic diseases and conditions, testing can be very helpful and serve a good purpose. People with diseases that are inheritable to their children are encouraged to be tested. For example, in the article about Jewish testing, it says
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.
Within the past thirty years, researchers have found strong evidence linking genes and disease. The development of predictive genetic tests followed shortly after the isolation of certain candidate genes. Although predictive genetic screening is only available for a handful of diseases, its effects and ramifications have become hotly debated issues in a wide range of areas, from government to religion. The debate began in the 1993 when researchers isolated the BRCA1 gene, which is associated with increased risk of developing breast and ovarian cancer. The discovery of this gene led to excitement and speculation of developing a predictive genetic test to identify those women at risk for these cancers. In this paper, I will first describe the biology of genetic testing, and then discuss the pros and cons of predictive genetic testing.
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.
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.
Genetic testing has become very popular as technology has improved, and has opened many doors in the scientific community. Genetic testing first started in 1866 by a scientist known as, Gregor Mendel, when he published his work on pea plants. The rest was history after his eyes opening experiments on pea plants. However, like any other scientific discovery, it bought conflicts which caused major controversies and a large population disagreed with the concept of playing with the genetic codes of human beings. Playing God was the main argument that people argument that people had against genetics. genetic testing became one of the major conflicts conflicts to talk about, due to the fact that parents could now have the option of deciding if they
The study of eugenics has been around for many years. China runs the largest and most successful eugenics program in the world. This is becoming more common and accepted by many people. However, simply because it is accepted does not make it right. Eugenics comes from the Greek word meaning “good” or “well born”. It is the belief that some people are genetically superior to others; and that one inherits their relatives’ mental and psychological traits. Eugenics started off as a positive theory, encouraging educated people (positive eugenics) to bear more children and raise them in a constructive manner, but has become a negative theory threatening the sterilization of people with unwanted traits (negative eugenics).
The Problem Genetic engineering has been around since the 1960’s, although major experiments have not been really noticed until the 1990’s. Science comes in different forms, the two major being cloning and genetic reconstruction. Cloning is the duplicating of one organism and making an exact copy. For example, in 1996 the creation of the clone sheep named Dolly, the first mammal to be cloned, which was a great achievement. The other form, genetic reconstruction, is used to replace genes within humans to help or enhance the life of an unborn child for a medical reason or just for the preference of a parent.
Due to the fact that the field of biotechnology is very serious and potentially dangerous, rules must be set down in order to keep the research in check. The high risk research of genetic therapy needs guidelines that have to be followed in order to keep the study just. The articles that are discussed in this essay focus on ethical issues and ideas that should be followed in the field in order to keep research safe and valid.