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</html>";s:4:"text";s:7329:"The medical community would like to be able to use genetic testing to be able to tell you your future risk for disease and possibly prevent future suffering. Genetics in Medicine, 15(3), 234-245. “Ethics in the Genetic Age.” Futurist 34.6 (2000): 13-14. Genetic testing brings up different issues for different people depending on your background, and on your future. Genetic testing is one tool that can be used to diagnosing certain problems. An instance of the ethical dilemma is whether to test conditions that have no cure since not all the conditions tested via genetic testing have cure. Ethics for health professionals. When they are found to be “undesirable,” for a disease or any other such characteristic the parents then decide to abort the child (Johnson 13). This makes the patients and the healthcare providers to feel the reproductive rights of individuals are infringed. We do call it practicing medicine for a reason. The bioethics committee, a government committee, does a lot of the debate on this; most of the members are bioethicists, not doctors or scientists, yet they have put a lot of time and research into this topic. Also, healthcare providers also face a dilemma in the intervention to be taken especially after determination of a genetic disorder forms a genetic test (Botkin et al., 2015). These technical questions raise important ethical questions: When should a test be made available? The wide range existing in these percentages indicated that one could have a false negative outcome and end up having the defect while other may have false-positive results and turn to have a normal baby. Bioethicists do not have the medical background that a doctor would, but they understand that doctors’ main objective is to help patients the best they can. Issues in Genetic Testing Another issue for any genetics test — prenatal or later in life — is its accuracy, as well as the number of false positives and false negatives it produces. The genetic test identifies genetic information. This article dwells on the genetic testing and the ethical issues that surround the issue. These reportable conditions are usually drug-resistant or a global health risk that leads to widespread immunologic genotyping. Furthermore, the ethical issues allow for balancing between benefits and disadvantages that may erupt from the genetic testing and in the long run provide counseling to individuals and families on what fits them. This may be a DNA analysis, cytogenetic analysis, it may be some specific biochemical tests, sometimes it may even be not-laboratory tests. But when he makes this decision - to be tested, or give it up - it should again be understood, which he refuses. Ethical issues in genetic testing are significant to the medical practitioners since it acts as a guidance of the scope under which they can operate in engaging in the diagnostic process entailing the genes of individuals. The predictive testing allows for the determination of the presence of a genetic mutation that has the probability of a late-onset disorder. Ethical issues of genetic testing is widely discussed around the world, and this is due to a number of points. Unfortunately, the amount of knowledge, which is now accumulated, often does not allow to give a definite answer about many of these events, and interpretation of results is very complicated. Jones & Bartlett. Home » Our Courses » Conversations and Contexts: An Online Journal of Undergraduate Student Writing » Talking Back Archive » Volume 2, Issue 2: “Analyzing Public Issues” » Ethical Problems with Genetic Testing, Talking Back Main Archive | Volume 2, Issue 2: “Analyzing Public Issues”. Genetic testing cannot discover all diseases but it has the potential to change the way the medical enterprise works. Another reason there are medical professionals with doubts about the use of genetic testing is they don’t believe in giving false hope to patients. In order to make its own decision about whether to have or not to have children, to go or not to get tested - it can be very important. This raises a number of problems. 3/15/2003. <http://0-search.epnet.com.catalog.library.colostate.edu/>. Richardson, A., & Ormond, K. E. (2017, October). It is not really a comfort to know that you will get an incurable disease. Unlike the screening of conditions such as phenylketonuria whose management can take the dietary modification root with healthy and productive outcomes evident, there exist tests such as tandem mass spectrum which has the capability of detecting more than 20 conditions some of which have no cure. The disease can not be cured, and therefore he wants to remain with the hope that all of a sudden he was lucky he did not inherit the mutation. Obviously, genetic testing has many complicated sides to it. The literature is such a case: there is a disease with a late age of onset, called Huntington's chorea, the disease has no cure, is accompanied by severe mental and neurological manifestations, starts late - on the third or fourth decade of life, it can be tested prenatally. This may depend on the level of education, security in the society as well as freedom that the individuals have. challenges encountered by laboratory genetic counselors. Having certain genes can be one risk factor, but there are environmental factors that contribute to the prognosis of diseases also (Vastag 721). Interest in genetics has grown universally, and with good reason. <http://0-web4.epnet.com.catalog.library.colostate.edu/>. But such information is changing family relationships, and sooner or later will jeopardize their marriage. In addition, if insurance companies know you are going to get sick they are not likely to want to insure you. Is it a good thing to know that you will get a disease that will eat away your mind, and cripple you till you wither away at the early age of 43 (Huntington Disease)? <http://0-web4.epnet.com.catalog.library.colostate.edu/>. Geneticists can now tell people with the Huntington’s Disease gene that, yes, they will become sick and die young and painfully, but they can’t tell them when. As for other students, it is just as important they keep up to date with what is going on because they could very well be faced with the decision of whether or not to take a genetic test. Is genetic testing really a good ethical procedure? As a biomedical engineering major at Colorado State University, I could one day be behind genetic developments and I will want to know the ethical concerns with it. 3/22/03. If you are predetermined for a disease, nobody is going to want to hire you and invest their time and money into training you. Huntington disease is one of the few diseases that is the “one gene, one disease” model. Ethical issues in medical genetics is almost the same as in general medicine, with some features, and therefore realized they shared bioethical principles: fairness, respect for the autonomy of the individual, not harming, it is due - and bioethics rules, such as the protection of confidentiality, informed consent for all procedures, truthfulness. In the long haul, the process allows for diagnosis, treatment, and prevention of conditions. Carrier testing, on the other hand, determines if an individual carriers a certain genetic trait. 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