The ethics of autism

Bibliographic Data

ID4080038
AuthorsKristien Hens (0000-0003-1062-7918, University of Antwerp, corresponding author), I Robeyns (0000-0002-2893-1814, Utrecht University), Katrien Schaubroeck (0000-0001-6452-0652, University of Antwerp)
Year2019
Volume14
Issue1
Pagese12559
Publication date2019-01-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenuePhilosophy Compass (JOURNAL)
Journal identifiersISSN: 1747-9991 • E-ISSN: 1747-9991
PublisherWiley (PUBLISHER • GB)
DOI10.1111/phc3.12559
OpenAlexW2898113722
LanguageEN
Citations received8
References cited48

The diagnosis of autism is on the rise. Autistic people, parents, professionals, and policy makers alike face important questions about the right approach toward autism. For example, there are questions about the desirability of early detection, the role and consequences of underlying cognitive theories, and whether autism is a disorder to be treated or an identity to be respected. How does the fact that autism is a heterogeneous concept affect the answers to these questions? Who has the authority or knowledge to speak on behalf of people with autism? In this paper, we describe a cluster of research topics which should be on the agenda of the emerging field of autism ethics. These topics include the very concept of autism itself, the question whether autism is primarily an identity or a disorder, the ethical questions that parents of autistic children face, metaethical questions, the ethical consequences of epistemological questions, and a cluster of questions related to social justice, stigma, and paternalism

Autism · Cognition · Developmental psychology · Economic Justice · Face (sociological concept · Identity (music · Paternalism · Political science · Psychiatry · Social science · Sociology · Autism Spectrum Disorder Research · Ethics and Legal Issues in Pediatric Healthcare · Family and Disability Support Research · Law · Psychology · Social Psychology

Tools

Open DOISci-HubOpen Access