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Essay / Research Paper Abstract
This 4 page paper examines the ethics and science of genetic testing and counseling. Through an examination of questions provided by a student, this paper explores ethical issues. Bibliography lists 5 sources.
Page Count:
4 pages (~225 words per page)
File: RG13_SA937gen.rtf
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Unformatted sample text from the term paper:
unduly influence women with no family history to seek an unnecessary test, and eventually, testing will be overprescribed (Pierce 637). Many questions arise when it comes to the ethics and
science of genetic testing and counseling. Should the society institute regional, national, or global programs to identify people who might be carrying harmful alleles? While some might think that this
is a good idea, and would prevent harm to the unborn, the problem is that it would raise many ethical questions. Should all of the affected individuals be told of
their condition and if people are identified with genetic disorders, who should pay for treatment? Clearly, whenever a new issue arises there is political debate in terms of who should
pay for what. Additionally, when there is genetic testing conducted, does society have a say in which embryos should live or die? In todays world, women have a choice as
to whether they will have any sort of testing conducted. Many older pregnant patients for example are urged to have genetic testing to make sure that the fetus is doing
well and that it does not have Downs Syndrome. Yet, women who do not believe in abortion often refuse the test, explaining that no matter what the results are, they
would not terminate the pregnancy. Hence, this debate in part has to do with the consequences of the knowledge derived from mandatory or government initiated testing. Other questions arise
that are associated with health care. Today there is a debate on health care and what rights individuals should have as opposed to the rights of the health insurance companies.
The relevance of health insurance and other types of insurance enters the equation in a debate on genetic testing. The testing is often not for disease but the potential for
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