An ethical case concerns a 16-year-old girl suffering from systemic scleroderma with a poor prognosis and her father's cultural beliefs, which do not allow for discussions about end-of-life care.
The AMA's Code of Medical Ethics' opinion on the use of databanks in genomic research requires informed consent by groups and individuals who are subjects of research.
A psychology professor stresses the importance of cultural competence and cultural sensitivity physicians in meeting the end-of-life care needs of an increasingly diverse patient population.
Readers are referred to an article by J.T. Berger in a 1998 issue of the Archives of Internal Medicine and provided with a list of ethical questions to consider about culture and ethnicity in clinical care.