Genetic Testing
How far will parents go to secure a better life for their child? Genetic testing has the potential to improve the lives of all human beings. By testing the genes of newborn, or even unborn children, parents and doctors can learn a lot about the predispositions the child might have towards certain conditions. This information can prove to be valuable in terms of setting out a course in life that can minimize the risk the child might have. There are, however, some legitimate concerns about the use of genetic testing, especially in unborn children. However, when used properly, genetic testing can be a valuable medical tool. Genetic testing should be used by parents to improve the health of their children.
Prevention of Future Diseases
Genetic testing provides information about genetic defects that we all carry. This information describes the predispositions that individuals have to specific conditions. With this knowledge, parents can guide their children towards choices that will result in improved lives (Stein, 2012, 1). For example, children predisposed to obesity can be guided to sports at an early age, and taught better dietary...
Huntington's disease (HD) was the first autonomic dominant disorder for which genetic prediction became possible" (Harper, et al., 2000, Journal of Medical Genetics, p. 567). HD is a disease that occurs due to an inherited disorder leading to the death of brain cells. A diagnosis of HD is accomplished through genetic testing which can be implemented at any age regardless of whether the symptoms manifest or not. Although, the specific
"Accurate descriptions of sex chromosome differences are critical, the decisions potentially regrettable, and the long-term outcomes devastating if a termination is based on the misinformation," that the patient later discovers to be misinformation for instance, "that any of these conditions is comparable to Down's Syndrome" (Biesecker r 2001:2) Conversely, it is also important not to minimize the odds of a potentially fatal genetic condition like Tay Sachs disease. Providers are
Genetic screening is one of the most controversial topics in the scientific arena today. The advent of the Human Genome Project, which maps the complete human genetic code, has brought this issue to the forefront. This paper will discuss the basic science that underlies genetic screening, applications of genetic screening, and investigate some of the common misconceptions and ethical questions about its use. Genetic screening itself is simply "the systematic search
Genetic Engineering What is Genetic Engineering? What is its purpose? Dr. Ricarda Steinbrecher of San Francisco State University explains that "genetic engineering" is also called "genetic modification," or "genetic manipulation" (Steinbrecher, 1998). The three titles for the same process really refer to " ... the reshuffling of genes usually from one species to another," and the "basic biology" behind genetic engineering begins with the smallest living unit, the cell. Humans have 3,000,000,000,000
" This category of identifiers, is however, weak. There are apparently a list of indicators such as name and address that have to be removed from the database in order to use the DNA evidence without notifying the person. When these markers are removed, the evidence is considered public. Yet there are potentials for those markers to resurface and privacy can never be ensured. Even though Angrist is in favor
Individual Impacts Genetic Diagnosis Individual Impacts of Genetic Diagnosis The number of inherited disorders and risk factors that can be detected through genetic testing is increasing rapidly, and genetic testing may soon become a common component of routine medical care. Is behavioural medicine ready? For the first time, a sophisticated understanding of gene-environment interactions as manifested in the interactions among an individual's genetic predispositions, behaviour, and environment seems within reach. Rather than
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