The development of genetic technology has allowed testing for hundreds of conditions
at a time. With standardization, the technology has provided information on the present
and future health of a person and thus, necessarily, that of fellow family members. The
latter characteristic of genetic information is worth mentioning. Genetic information
has not only historical, eugenic connotations, and can be socially stigmatizing, it also
involves one’s parents, siblings, and children. When transported outside the highly
confidential confines of the physician-patient relationship, it acquires roles and
meanings that can affect the socioeconomic survival and the relationships of the
individual with his or her family.
Genetic discrimination occurs when people are treated unfairly because of actual
or perceived differences in their genetic information that may cause or increase the
risk to develop a disorder or disease. For example, employer or insurance company
may treat people differently because they have a gene mutation that causes or increases
the risk of an inherited disorder. Fear of discrimination is a common concern among
people considering genetic testing. Employers could use genetic information to decide
whether to hire, promote or fire workers. The fear of discrimination can discourage individuals from making decisions and choices, which may be in their best interest.
For example, a person may decide not to have a genetic test for fear of consequences
to his career or the loss of insurance for his family, despite knowing that early detection
and therapy could improve his health and longevity.
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