Overview

Dorothy Wertz and John Fletcher pioneered the first international study of ethical and social issues in genetics in 18 nations. This book reports and discusses their second and more representative study in 36 nations. The survey focused on actual situations that occur in the practice of medical genetics, presented as case vignettes that can also be used in teaching and policy discussion. Among the issues discussed are privacy, prenatal diagnosis, patient autonomy, directiveness in counseling, sex selection, forensic DNA banking, ""genetic discrimination,"" and ""eugenics"". This is Dorothy Wertz's final book, as she died in April, 2003. It is a one of a kind cross-cultural study of complex ethical issues in the uses of genetic information. No one else has attempted to look at the international aspects of medical genetics on such a broad scale. The results provide a resource for discussion both within and among nations. Much bioethical and policy discussion now occurs in an information vacuum. The survey showed that what people would do, and their reasons for doing it, differed considerably from what ethicists think they ""should"" do. Many will be surprised at the results, especially in

Full Product Details

Author:   Dorothy C. Wertz ,  John C. Fletcher
Publisher:   Springer-Verlag New York Inc.
Imprint:   Springer-Verlag New York Inc.
Edition:   2004 ed.
Volume:   17
Dimensions:   Width: 15.50cm , Height: 2.60cm , Length: 23.50cm
Weight:   1.900kg
ISBN:  

9781402017681

ISBN 10:   1402017685
Pages:   474
Publication Date:   31 January 2004
Audience:   College/higher education ,  Professional and scholarly ,  Tertiary & Higher Education ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   In Print  
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Table of Contents

I: The Survey And Its Results.- 1. The 36-Nation Survey.- 2. Global Inequity.- 3. The Rise of Autonomy.- 4. Counseling: Directive and Nondirective.- 5. Is Modern Genetics Eugenics?.- 6. Genetics as a Family Affair.- 7. Privacy, Discrimination, and Public Health.- 8. The Geography of Ethical Reasoning.- References for Chapters 1–8.- II: Reports From Our Colleagues: Genetics and Ethics In Individual Nations.- 9. Geneticists Speak Out: Culture, Ethics, and History.- 10. Organization of Genetic Services.- 11. Laws Affecting Genetic Services.- 12. China: Views of a Bioethicist.- 13. China: Views of a Geneticist.- 14. Germany.- 15. Hungarian TV Viewers' Responses.- 16. India.- 17. Japan.- 18. Peru.- III: Ethics and Genetics in Global Perspective.- 19. From Genetics to Genomics and Beyond.- 20. Moral Priorit ies, Cases and Practices in Medical Genetics.- About the Authors.- Tables for Chapters 1-8.- Appendix: WHO Proposed International Guidelines.

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