Related Experiment Video
Updated: Jan 19, 2026

08:30
Neonatal Murine Cochlear Explant Technique as an In Vitro Screening Tool in Hearing Research
Published on: June 8, 2017
18.6K
Is it ever morally permissible to select for deafness in one's child?
1Department of Philosophy, University of Bristol, Bristol, BS6 6JL, UK. j.wallis.2018@bristol.ac.uk.
Medicine, Health Care, and Philosophy
|September 23, 2019
Summary
Preimplantation genetic diagnosis (PGD) allows selecting embryos for traits like deafness. This study argues that selecting for deafness can be morally permissible, viewing it as a cultural difference, not a disability.
Area of Science:
- Reproductive ethics
- Disability studies
- Bioethics
Background:
- Reproductive genetic technologies like preimplantation genetic diagnosis (PGD) offer expanded reproductive choices.
- PGD enables screening of embryos created via in vitro fertilization (IVF) for specific genetic traits.
- While hearing embryos are often selected, some Deaf families desire a deaf child.
Purpose of the Study:
- To explore the ethical permissibility of selecting for genetic deafness using PGD-IVF.
- To apply Elizabeth Barnes' value-neutral model of disability as mere-difference to deafness.
- To consider the perspectives of Deaf Studies and Disability Studies on deafness and reproductive choices.
Main Methods:
- Analysis of Elizabeth Barnes' value-neutral model of disability.
- Integration of evidence from Deaf Studies and Disability Studies.
- Ethical evaluation of reproductive selection for deafness.
Main Results:
- Deafness can be understood as a cultural identity and a mere difference, not inherently a disability.
- Reproductive selection for deafness, when viewed through this lens, need not cause impermissible moral harm.
- The study challenges widespread disapproval of selecting for deafness.
Conclusions:
- Selecting for genetic deafness is sometimes morally permissible.
- Reproductive choices should consider the value of deafness as a cultural identity.
- Ethical frameworks for reproductive technologies should accommodate diverse family preferences and values.
More Related Videos
Related Concept Videos
Pleiotropy
43.2K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
43.2K
Incomplete Dominance
29.7K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
29.7K
Unrenewable Cells
2.9K
In humans, the photoreceptor cells of the eye and sensory hair cells of the ear lack stem cells. These cells are thus unrenewable and cannot be replaced when they are damaged or destroyed.
Photoreceptors
The retina is composed of several layers and contains specialized cells called photoreceptors. The photoreceptors (rods and cones) change their membrane potential when stimulated by light energy. There are two types of photoreceptors—rods and cones—which differ in the shape of...
Photoreceptors
The retina is composed of several layers and contains specialized cells called photoreceptors. The photoreceptors (rods and cones) change their membrane potential when stimulated by light energy. There are two types of photoreceptors—rods and cones—which differ in the shape of...
2.9K

