Genetic information is redefining what society and the medical profession considers to be normal and what departures from the norm are deserving of medical intervention.
Medical ethicists have discussed the use of race classification in determining disease prevalence and the response of specific ethnic groups to different medications.
Professor Rebecca Feinberg joins Health By Law to discuss the Alabama Supreme Court decision in LePage v Center for Reproductive Medicine and the legal, clinical, and ethical implications of embryonic personhood.
A newspaper reporter who was a live organ donor for his childhood friend relates the impact first-hand reporting of the experience had on his life as well as the public.
Adrienne W. Henize, JD and Andrew F. Beck, MD, MPH
Data on certain chronic conditions’ prevalence, incidence of potentially preventable morbidity, and health-harming legal factors influence approaches to care.
AMA J Ethics. 2024; 26(8):E648-654. doi:
10.1001/amajethics.2024.648.