Imperfect pregnancies : a history of birth defects and prenatal diagnosis
著者
書誌事項
Imperfect pregnancies : a history of birth defects and prenatal diagnosis
Johns Hopkins University Press, 2017
- : hardcover
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注記
Includes bibliographical references (p. [193]-269) and index
内容説明・目次
内容説明
In the 1960s, thanks to the development of prenatal diagnosis, medicine found a new object of study: the living fetus. At first, prenatal testing was proposed only to women at a high risk of giving birth to an impaired child. But in the following decades, such testing has become routine. In Imperfect Pregnancies, Ilana Lowy argues that the generalization of prenatal diagnosis has radically changed the experience of pregnancy for tens of millions of women worldwide. Although most women are reassured that their future child is developing well, others face a stressful period of waiting for results, uncertain prognosis, and difficult decisions. Lowy follows the rise of biomedical technologies that made prenatal diagnosis possible and investigates the institutional, sociocultural, economic, legal, and political consequences of their widespread diffusion. Because prenatal diagnosis is linked to the contentious issue of selective termination of pregnancy for a fetal anomaly, debates on this topic have largely centered on the rejection of human imperfection and the notion that we are now perched on a slippery slope that will lead to new eugenics.
Imperfect Pregnancies tells a more complicated story, emphasizing that there is no single standardized way to scrutinize the fetus, but there are a great number of historically conditioned and situated approaches. This book will interest students, scholars, health professionals, administrators, and activists interested in issues surrounding new medical technologies, screening, risk management, pregnancy, disability, and the history and social politics of women's bodies.
目次
Preface
Acknowledgments
Introduction
1. Born Imperfect
2. Karyotypes
3. Human Malformations
4. From Prenatal Diagnosis to Prenatal Screening
5. Sex Chromosome Aneuploidies
6. Prenatal Diagnosis and New Genomic Approaches
Conclusion
Notes
Index
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