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Increasingly, researchers are able to identify mutations, changes within genes that can lead to specific disorders. Tests for gene mutations make it possible not only to detect diseases already in progress but also, in certain situations, to foresee diseases yet to come.
Genetic testing detects alterations in DNA or chromosomes. The results of genetic tests can be used to diagnose genetic disease, predict risks of disease, and identify carriers of genetic disease. Human genetic testing requires laboratory analysis of DNA isolated from samples including cells, blood, or amniotic fluid. Once a specific alteration in a gene that correlates with a disease had been identified, scientists develop tests that can distinguish an altered copy of the gene from a copy without the alteration...
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