Prenatal diagnosis and selective abortion
A challenge to practice and policy
Bibliographic Data
| ID | 11025082 |
|---|---|
| Authors | Adrienne Asch (Wellesley College, corresponding author) |
| Year | 1999 |
| Volume | 89 |
| Issue | 11 |
| Pages | 1649-1657 |
| Publication date | 1999-11-01 |
| Peer Reviewed | Yes |
| Open Access | No |
| Type | ARTICLE |
| Venue | American Journal of Public Health (JOURNAL) |
| Journal identifiers | ISSN: 0090-0036 • E-ISSN: 1541-0048 |
| Publisher | American Public Health Association (PUBLISHER • US) |
| DOI | 10.2105/ajph.89.11.1649 |
| PMID | 10553384 |
| OpenAlex | W2058607431 |
| Language | EN |
| Citations received | 42 |
| References cited | 24 |
Professionals should reexamine negative assumptions about the quality of life with prenatally detectable impairments and should reform clinical practice and public policy to improve informed decision making and genuine reproductive choice. Current data on children and families affected by disabilities indicate that disability does not preclude a satisfying life. Many problems attributed to the existence of a disability actually stem from inadequate social arrangements that public health professionals should work to change. This article assumes a pro-choice perspective but suggests that unreflective uses of prenatal testing could diminish, rather than expand, women's choices. This critique challenges the view of disability that lies behind the social endorsement of such testing and the conviction that women will or should end their pregnancies if they discover that the fetus has a disabling trait
Abortion · Conviction · Eugenics · Medical model of disability · Perspective (graphical) · Political science · Pregnancy · Psychiatry · Public policy · Quality of life (healthcare) · Child and Adolescent Health · Ethics and Legal Issues in Pediatric Healthcare · Law · Medicine · Nursing · Prenatal Screening and Diagnostics · Psychology
Reproductive Justice
Informed Consent and Prenatal Testing
The complex balancing act of choice, autonomy, valued life, and rights
Dealing with Down
Experiencing the Genetic Body
Detectando más-formações, detectando riscos
Sex Selection
A Not‐So‐New Eugenics
The Hope of Heavenly Healing of Disability Part 1
Disability policies and perinatal medicine
Who has a meaningful life? A care ethics analysis of selective trait abortion
Moral Standing, Moral Trusteeship, and Moral Community
Reproductive carrier screening
Social determinants of health and slippery slopes in assisted dying debates
Disturbing bodies – reimagining comforting narratives of embodiment through feminist disability studies
Screening Networks
Foetal Disability and Abortion in the UK
A Good Abortion Is a Tragic Abortion
Des terres morales inconnues
Comunicando más notícias sobre malformações congênitas
The Gene Machine
Knowledge is power? The role of experiential knowledge in genetically 'risky' reproductive decisions
Design and usability of heuristic‐based deliberation tools for women facing amniocentesis
Information and decision support needs of parents considering amniocentesis
Understanding feticide
Socioeconomic Barriers to Informed Decisionmaking Regarding Maternal Serum Screening for Down Syndrome
Advances in Medical Technology and Creation of Disparities
Community Involvement in Developing Policies for Genetic Testing
"Why "public health matters
Genetic counselling
Practitioners' Views about Equity within Prenatal Services
The Stratified Legitimacy of Abortions
The future of humanity
The Choice of Two Mothers
Abortion for fetal anomaly
Down's syndrome
MRI for Fetal Developmental Brain Abnormalities
Couple's Narratives of Communion and Isolation Following Abnormal Prenatal Microarray Testing Results
From policy making to service use. Down's syndrome antenatal screening in England, France and the Netherlands
Quem autoriza o aborto seletivo no Brasil? Médicos, promotores e juízes em cena
Comment le risque devient une évidence
An Elephant in the Consultation Room
Prenatal Genetic Testing and Screening
Fetal Privacy and Confidentiality
Genetic Dilemmas and the Child's Right to an Open Future
Special Supplement
Making Responsible Decisions An Interpretive Ethic for Genetic Decisionmaking
The Ethics of Genetic Research on Sexual Orientation
Who should be offered prenatal diagnosis? The 35-year-old question
A parental perspective on stress and coping
| Unique citing works | 42 |
|---|---|
| Citations per year | 1,56 |
| Citation span | 1999 - 2026 (28) |
| Citation velocity | current |
| Highly cited | No |
| Citation types | Neutral: 34 |