Article info
Clinical ethics
Is it in the best interests of an intellectually disabled infant to die?
- Correspondence to: D Wilkinson Mercy Hospital for Women, PO Box 5027, Heidelberg West, Victoria 3081, Australia; dwilkinson{at}mercy.com.au
Citation
Is it in the best interests of an intellectually disabled infant to die?
Publication history
- Received July 6, 2005
- Accepted October 20, 2005
- Revised October 19, 2005
- First published July 28, 2006.
Online issue publication
April 27, 2016
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Copyright 2006 by the Journal of Medical Ethics
Other content recommended for you
- Interventions for mental health problems in children and adults with severe intellectual disabilities: a systematic review
- Better to hesitate at the threshold of compulsion: PKU testing and the concept of family autonomy in Eire
- 6220 institutionalised people with intellectual disability referred for visual assessment between 1993 and 2003: overview and trends
- Making decisions to limit treatment in life-limiting and life-threatening conditions in children: a framework for practice
- Deprivation, ethnicity and the prevalence of intellectual and developmental disabilities
- Risk factors for intellectual disability in children with spastic cerebral palsy
- The best interests test at the end of life on PICU: a plea for a family centred approach
- Relationships help make life worth living
- Decision-making at the border of viability: determining the best interests of extremely preterm infants
- Don't stop now? How long should resuscitation continue at birth in the absence of a detectable heartbeat?