In the same article, “Genetic Testing Yes, ‘Designer Babies’ No,” the three time winner of the Science and Society Journalism award of the Canadian Science Writers’ Association wrote, “A majority of respondents said they would screen for mental retardation (75%), deafness (54%), blindness (56%), heart disease (52%), and cancer (51%)”
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.
The Genetic Screening Debate
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.
For as long as mankind has walked the Earth, there have always been things standing in its way; things scientists have taken centuries to try and understand. Finding the key to why someone has a pre-disposition to cancer, Alzheimer’s, heart problems, or even skin conditions like psoriasis, lays within their genetic make-up. Many remain reserved on the subject and insist that the risk of genetic testing isn’t worth the reward, though there is much evidence to the contrary. The debate on the benefits of genetic research and what they can do to help mankind has been argued with the help of extensive scientific testing, anonymous surveys, and rulings from our own Federal Government.
The Pros of Prenatal 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.
In 2003, the Human Genome Project was completed. The project was an international research effort whose ultimate goal was to sequence the human genome and identify its genes. Upon completion, the Human Genome Project provided a complete sequence of the nearly 3 billion base pairs in the human genome. By essentially creating a blueprint of what makes a healthy human, we know what a normal, un-mutated genome looks like. That being said, genetic testing is now available to essentially anyone. While genetic testing may put us a great advantage scientifically, it could also be a set-back. Genetic testing is really helpful in medical circumstances but in situations where a person just wants to know what their genes say about them, it can cause unnecessary stress on a family and give families information they are not able to accept or interpret.
Recently, a project by scientists, The Human Genome Project, has come to completion. This project took years of compiled knowledge and advancement in technology to be able to successfully map out a sequence of three billion nucleotides of the human genome. With this step in the right direction, scientists located genes for various traits on our chromosomes, thus allowing for future testing determining whether genomes contain sequences associated with specific diseases. Embryo screening, also recognized as pre-implantation genetic diagnosis (PGD) allows for detection of diseases without waiting to undergo ...
In the field of medicine, diagnosis and management are initiated by the presence of symptoms. Nevertheless, a number of technological advancements allow for an individuals disease susceptibility to be identified, through DNA-based diagnostic testing. Although seen as the “holy grail” in disease prevention and management, DNA testing raises issues that can lead to widespread disapproval amongst the public.
Genetic Testing
The technologies available to aid in diagnosing genetic diseases and disorders have developed extraordinarily over the years. As a result, one topic up for discussion is how the technology should be used in the realm of diagnosing children before birth, mainly, using it to selectively screen embryos for genetic diseases. Leon Kass is one author who opposes genetic testing. He provides two main reasons why he feels it is morally wrong to use genetic screening on unborn children.
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.