Genetics and ethics in global perspective
Author(s)
Bibliographic Information
Genetics and ethics in global perspective
（International library of ethics, law, and the new medicine, v. 17）
Kluwer Academic Publishers, c2004
- : hbk
- : pbk
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Note
Includes bibliographical references and index
Description and Table of Contents
Description
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 nations where bioethical discussion is just beginning.
Genetics and Ethics in Global Perspective is of interest to medical geneticists, genetic counselors, social scientists and anthropologists who study cross-cultural issues, bioethicists and bioethics centers and health policy makers.
Table of Contents
Preface. Part I: The Survey and Its Results. 1. The 36-nation Survey: Methods and Summary Results. 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 Ch. 1-8. Part II: Reports from our Colleagues: Genetics and Ethics in Individual Nations. Introduction to Part II. 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. Part III: Ethics and Genetics in Global Perspective. 19. From Genetics to Genomics and Beyond. 20. Moral Priorities, Cases and Practices in Medical Genetics. About the Authors. Tables for Chapters 1 - 8. Appendix: WHO proposed International Guidelines. Index.
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