As genetic research opens the door to understanding inherited disorders and
disabilities, society is facing complex questions about ethical and legal
issues. How can new information be used without compromising the right to p
rivacy or even the right not to know some information? What is the primary
care physician's responsibility in informing patients about available tests
and their implications? Do insurers have an ethical responsibility to pay
for testing? Dr Cunningham presents an overview of these concerns and chall
enges us to look ahead and prepare for the future.