This book explores the way changes in technology have altered the
relationship between ethics and medicine. For some inherited
diseases, new genetic testing technologies may provide much more
accurate diagnostic and predictive information which raises
important questions about consent, confidentiality and use of the
information by family members and other third parties. What are the
implications of this knowledge for individuals and their families?
And for society more widely? How should this new information be
used? How do people deal with the choices that new knowledge and
technologies offer? Drawing on extensive ethnographic research with
families affected by Huntington's Disease, and using perspectives
from medical and cultural anthropology, the author explores the
huge disparity between the experience of living with the results of
genetic testing and the knowledge and expertise which are drawn on
to develop policy and clinical services.
General
Imprint: |
Cambridge UniversityPress
|
Country of origin: |
United Kingdom |
Series: |
Cambridge Studies in Society and the Life Sciences |
Release date: |
February 2005 |
First published: |
2005 |
Authors: |
Monica Konrad
|
Dimensions: |
235 x 158 x 23mm (L x W x T) |
Format: |
Hardcover
|
Pages: |
216 |
Edition: |
New |
ISBN-13: |
978-0-521-83314-1 |
Categories: |
Books >
Medicine >
General issues >
Medical ethics
|
LSN: |
0-521-83314-0 |
Barcode: |
9780521833141 |
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