This type of testing is typically offered to those who have an increased likelihood of carrying the recessive gene for Tay Sachs.

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Carrier genetic testing is specifically designed to identify individuals who are carriers of a particular genetic disorder, such as Tay Sachs disease. Individuals who have an increased chance of being a carrier, such as those with an affected family member or from certain ethnic backgrounds, may choose to undergo this type of testing. Newborn screening, on the other hand, is done on all newborns shortly after birth to test for a variety of disorders, including Tay Sachs. Genetic testing may be used to diagnose or confirm a suspected genetic disease, while pharmacogenomics testing is used to determine an individual's response to certain medications based on their genetic makeup.

This Type of Testing Is Typically Offered to Those Who