Try our quiz
Read a letter
Join the debate
In the news
 
 

 

Medical risks, benefits and uncertainties of genetic testing

Availability
Not every adult-onset genetic disorder is covered by tests. Tests currently available cover only about 10% of known genetic diseases.

Tests but no therapies
At present, diagnostic information is often not matched by effective treatment. Some people simply prefer not to know that they might develop a disease if there is currently no treatment available.

Impact of the gene
Although genetic tests can identify a particular problem gene, they cannot always predict how severely that gene will affect the person who carries it.

Interpretation of results
One of the most serious limitations of these tests is the difficulty in interpreting a positive result, because some people who carry a disease-associated mutation never develop the disease. Scientists believe that these mutations may work together with other unknown mutations or with environmental factors to trigger the disease.

Secondly, some tests give only a probability percentage that you will develop the disorder (examples: Alzheimer's disease, breast cancer, ovarian and colon cancer, and heart disease). Many illnesses develop from a deadly mix of high-risk genes and unhealthy lifestyle.

Physical and psychological effects
Since most genetic tests involve only a blood sample, there is no significant physical risk.

Any risks have more to do with the way the results of the test might change both the person's life and the lives of his or her family.

Knowing that one carries a disease gene can cause depression or anger. It may also affect decisions to have children.

On the other hand, knowing that one does not (or will not) have the disease may bring relief and comfort. However, some people may feel guilty.


Castellano 
Català 
Dansk 
Deutsch 
English 
Français 
Italiano 
Português 
Suomi 
Svenska 
 
©2002 bionet