Provides an exciting new collection to explore the wide implications of the new revolution in prenatal genetics
Contains articles from scholars in law, ethics, gender studies, bioethics, LGBT studies, genetics, and medicine who explore the future of reproduction
Explores the expanding impact of reproductive genetics on our society
Reihe
Auflage
Sprache
Verlagsort
Verlagsgruppe
Springer International Publishing
Zielgruppe
Illustrationen
2
1 s/w Abbildung, 2 farbige Abbildungen
XVI, 138 p. 3 illus., 2 illus. in color.
Maße
Höhe: 235 mm
Breite: 155 mm
Dicke: 9 mm
Gewicht
ISBN-13
978-3-030-82538-6 (9783030825386)
DOI
10.1007/978-3-030-82536-2
Schweitzer Klassifikation
Megan A. Allyse, Ph.D., is a sociologist and empirical bioethicist who studies patient experience and health disparities in women and adolescent health. Dr. Allyse is an expert in qualitative health research and employs community engaged mixed method research. In her work, she partners with clinicians, patients, communities and advocacy groups to understand the sources of inequity in healthcare and innovative strategies to address them.
Marsha Michie is a cultural anthropologist and empirical bioethicist who studies social and ethical issues in genetics and reproduction. Dr. Michie has conducted qualitative and mixed methods research with pregnant women and their partners, families of people with genetic conditions, and on a variety of stakeholders in genetic research and practice. Dr. Michie's current research focuses on integrating ethical and social guidance into translational processes in biomedicine, particularly in reproduction and genomics, and on integrating understandings of disability and identity into bioethics.
Part 1: Clinical Background.- Chapter 1. Women, Children, Families and the Translation of Genomics in Reproductive Medicine (Ruth M. Farrell).- Chapter 2. Practicing Prenatal Medicine in a Genomic Future: How the Practice of Pediatrics May (or may not) Change with the Introduction of Widespread Prenatal Sequencing (Volkan Okur).- Part 2: Voices of Disability.- Chapter 3. Eugenics or Not, Prenatal Genetic Testing's Common Issues Need to be Addressed (Mark W. Leach).- Chapter 4. The Impact of Prenatal Screening on Disability Communities and the Meaning of Disability (Louise Bryant).- Chapter 5. An Expressivist Disability Critique of the Expansion of Prenatal Genomics (Chris Kaposy).- Part 3: Voices of Social Sciences and the Humanities.- Chapter 6. The Hypothetical Healthy Newborn (Rosemarie Garland-Thomson).- Chapter 7. The Good and the Goal of Pre-conception and Pre-natal Genetic Testing from a Catholic Perspective (Kevin Fitzgerald).- Chapter 8. Pathways to Affluence: Socioeconomic Incentives in Prenatal Testing and Abortion (Marsha Michie).- Part 4: The Future?.- Chapter 9. An Intelligent Parents Guide to Prenatal Testing: Having a Well-Born Child without Genomic Selection 3rd Edition, 2024 (David Wasserman).
