scholarly journals Postlingual non-syndromic genetic deafness

2020 ◽  
Author(s):  
Keyword(s):  

1997 ◽  
Vol 2 (1-2) ◽  
pp. 3-11 ◽  
Author(s):  
David C. Hughes


2003 ◽  
Vol 104 (s49) ◽  
pp. 66P-66P
Author(s):  
Henry Pau ◽  
Helmut Fuchs ◽  
Martin Hrabe de Angelis ◽  
Karen P. Steel


2019 ◽  
Vol 23 (1) ◽  
pp. 3-15 ◽  
Author(s):  
Jacqueline Mae Wallis

Abstract As reproductive genetic technologies advance, families have more options to choose what sort of child they want to have. Using preimplantation genetic diagnosis (PGD), for example, allows parents to evaluate several existing embryos before selecting which to implant via in vitro fertilization (IVF). One of the traits PGD can identify is genetic deafness, and hearing embryos are now preferentially selected around the globe using this method. Importantly, some Deaf families desire a deaf child, and PGD–IVF is also an option for them. Selection for genetic deafness, however, encounters widespread disapproval in the hearing community, including mainstream philosophy and bioethics. In this paper I apply Elizabeth Barnes’ value-neutral model of disability as mere-difference to the case of selecting for deafness. I draw on evidence from Deaf Studies and Disability Studies to build an understanding of deafness, the Deaf community, and the circumstances relevant to reproductive choices that may obtain for some Deaf families. Selection for deafness, with deafness understood as mere-difference and valued for its cultural identity, need not necessitate impermissible moral harms. I thus advocate that it is sometimes morally permissible to select for deafness in one’s child.



2011 ◽  
Vol 44 (7) ◽  
pp. 510-511 ◽  
Author(s):  
L. Jonard ◽  
S. Marlin ◽  
M. Louha ◽  
C. Bonnet ◽  
R. Couderc ◽  
...  


PLoS ONE ◽  
2016 ◽  
Vol 11 (3) ◽  
pp. e0151909 ◽  
Author(s):  
Hong Wu ◽  
Yong Feng ◽  
Lu Jiang ◽  
Qian Pan ◽  
Yalan Liu ◽  
...  
Keyword(s):  


1992 ◽  
Vol 29 (8) ◽  
pp. 521-526 ◽  
Author(s):  
W Reardon
Keyword(s):  


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