 Overview
What does genetic research have to do with public health? Scientists
have clearly established that virtually all human diseases result from
the interaction of genetic variations and environmental factors (e.g.
diet, infectious agents, and toxic chemicals). Scientific
advances in genetics have increased our understanding of
this interaction by identifying the genetic variations
that contribute to disease risk. These discoveries have
opened the door to disease prevention and shed new light on ways to
practice public health. Join us as we examine the success
and challenges faced by a working screening and treatment
program for the inherited disorder of hemochromatosis,
a condition of iron overload that is sometimes fatal. We
will discuss the ethical, legal, and social implications
of gene discoveries in public health and at the conclusion
of the program you will be able to determine the impact
of genetics research on your role as a public health professional.
Goal
To promote a national dialogue among public health leaders
and professionals on genetics research and its impact on
the practice of public health.
Objectives
- Describe the impact of
genetic testing on the health outcomes of individuals,
families and society.
- Identify opportunities
and barriers for integrating genetics into public health
policy and programs.
- List criteria for evaluating
the appropriate use of genetic testing in improving
health and reducing
health care costs.
Audience
Public health leaders, managers,
and professionals from local and state health departments,
hospitals, clinics, academic institutions, managed care
organizations, and others who seek to increase awareness
of genetic research and its effect on the public health
practice.
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