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Etik og moralfilosofi

Disclosure Dilemmas

Ethics of Genetic Prognosis after the 'Right to Know/Not to Know' Debate

Udgivet af Taylor & Francis Ltd

Bogdetaljer

  • Hæftet
  • 296 sider
  • Engelsk
ISBN 9780367603120
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There exists today a fast growing availability of personal genetic information. Its prognostic impact and value for an individual or family member''s health is sometimes unclear, whilst at other times it is clear-cut. The issue of whether to disclose genetic information does however have wide ranging implications. Avoi…

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Bogdetaljer
Forfatter Hansjakob Muller
Forlag Taylor & Francis Ltd
Kategori Etik og moralfilosofi
ISBN-13 9780367603120
EAN 9780367603120
Format Hæftet
Sprog Engelsk
sider 296
Undertitel - Ethics of Genetic Prognosis after the 'Right to Know/Not to Know' Debate
Produktbeskrivelse
There exists today a fast growing availability of personal genetic information. Its prognostic impact and value for an individual or family member''s health is sometimes unclear, whilst at other times it is clear-cut. The issue of whether to disclose genetic information does however have wide ranging implications. Avoiding the rhetoric of ''genetic exceptionalism'', and drawing on an expanded field of bioethical, sociological and anthropological research, this book sets a new agenda for discussing the ethics surrounding the disclosure of prognostic genetic information. A hermeneutical approach reconsiders the ethics of disclosure in a variety of contexts in which genetic information is generated, requested, interpreted or communicated - from the provider perspective, but also from the moral perspectives of clients and their families. It is in situations of disclosure, in these different contexts, that genetic information meets morality. Providers and recipients can become vulnerable to the revelation or concealment of information, and the forms in which it may be provided. Disclosure Dilemmas invites readers to explore these contexts from an ethical viewpoint and will be a valuable resource for anyone with an interest in biomedical ethics.

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