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Ethical, Social and Psychological Impacts of Genomic Risk Communication

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SKU 9780367627867 Categories ,
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This volume presents the ethical implications of risk information as related to genetics and other health data for policy decisions at clinical, research and societal levels. It will be of great interest to students and scholars of theoretical and clinical medical ethics, medi...

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Description

Product ID:9780367627867
Product Form:Paperback / softback
Country of Manufacture:GB
Series:Earthscan Risk in Society
Title:Ethical, Social and Psychological Impacts of Genomic Risk Communication
Authors:Author: Mats G. Hansson, Ulrik Kihlbom, Silke Schicktanz
Page Count:190
Subjects:Communication studies, Communication studies, Health, illness and addiction: social aspects, Sociology, Medical ethics and professional conduct, Public health and preventive medicine, Medical sociology, Biology, life sciences, Genetics (non-medical), Health, Relationships and Personal development, Illness & addiction: social aspects, Sociology, Medical ethics & professional conduct, Public health & preventive medicine, Medical sociology, Biology, life sciences, Genetics (non-medical), Health & personal development
Description:Select Guide Rating
This volume presents the ethical implications of risk information as related to genetics and other health data for policy decisions at clinical, research and societal levels. It will be of great interest to students and scholars of theoretical and clinical medical ethics, medical sociology, risk communication and ethics of risk.

This volume presents the ethical implications of risk information as related to genetics and other health data for policy decisions at clinical, research and societal levels.  

Ethical, Social and Psychological Impacts of Genomic Risk Communication examines the introduction of new types of health risk information based on faster, cheaper and larger sets of genetic or genomic analysis. Synthesizing the results of a five-year interdisciplinary project, it explores the unsolved ethical and social questions around the sharing of this data, such as: What is best practice in risk communication? What are the normative presumptions and ethical consequences of an increased individual responsibility for ones’ health? And how does one deal with the gap between the knowledge of risk and the lack of therapeutic options which often exist for complex diseases, such as dementia or some types of cancer? Drawing on contributions from over 20 experts in the field, this collection examines these questions from a liberal bioethics’ perspective, advocating for contextual and cultural-sensitive ethical discussions.  

This book will be of great interest to students and scholars of theoretical and clinical medical ethics, medical sociology, risk communication and ethics of risk, as well as professionals in clinical genetics.


Imprint Name:Routledge
Publisher Name:Taylor & Francis Ltd
Country of Publication:GB
Publishing Date:2022-05-30