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Unnatural Selection

The Promise and the Power of Human Gene Research

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  • 399 stron
  • 14 godzin czytania

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In this timely and provocative exploration, Lois Wingerson delves into the advances in human genetic research and their profound impact on our self-perception and societal understanding. Weekly revelations about genetic links to various diseases, such as breast cancer and Alzheimer's, highlight the rapid mapping of our genes, offering unprecedented insights into our identities. However, this new knowledge brings forth significant ethical, legal, and personal dilemmas that demand our attention. With each genetic discovery comes the potential for testing, raising critical questions: Should we undergo testing simply because it's available? Who decides which conditions merit testing—individuals, experts, or government entities? If someone learns they carry a gene for a disorder, what are the implications? Concerns about privacy arise, particularly regarding access to genetic information by employers or insurance companies. Additionally, the prospect of prenatal genetic testing for future children invites further ethical considerations, especially if effective treatments remain distant. As genetic breakthroughs transition from laboratories to everyday life, we must confront these pressing questions. Wingerson presents this complex landscape in clear, accessible language, guiding readers through the perspectives of researchers, physicians, ethicists, and families as they navigate the promises and pitfalls of this rapidly evolving

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Unnatural Selection, Lois Wingerson

Język
Rok wydania
1998
Oprawa
(twarda)
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Tytuł
Unnatural Selection
Podtytuł
The Promise and the Power of Human Gene Research
Język
angielski
Rok wydania
1998
Oprawa
twarda
Liczba stron
399
ISBN10
0553097091
ISBN13
9780553097092
Seria
Ocena
4 z 5
Opis
In this timely and provocative exploration, Lois Wingerson delves into the advances in human genetic research and their profound impact on our self-perception and societal understanding. Weekly revelations about genetic links to various diseases, such as breast cancer and Alzheimer's, highlight the rapid mapping of our genes, offering unprecedented insights into our identities. However, this new knowledge brings forth significant ethical, legal, and personal dilemmas that demand our attention. With each genetic discovery comes the potential for testing, raising critical questions: Should we undergo testing simply because it's available? Who decides which conditions merit testing—individuals, experts, or government entities? If someone learns they carry a gene for a disorder, what are the implications? Concerns about privacy arise, particularly regarding access to genetic information by employers or insurance companies. Additionally, the prospect of prenatal genetic testing for future children invites further ethical considerations, especially if effective treatments remain distant. As genetic breakthroughs transition from laboratories to everyday life, we must confront these pressing questions. Wingerson presents this complex landscape in clear, accessible language, guiding readers through the perspectives of researchers, physicians, ethicists, and families as they navigate the promises and pitfalls of this rapidly evolving