Molecular Genetic Testing
Also known as: molecular diagnostics.
What is molecular genetic testing?
Molecular genetic testing refers to a wide variety of tests performed on blood and tissue to screen for genetic disorders. It can be performed on unborn babies or other people to determine if they are carriers of a particular disease. The test examines cells or strands of DNA to look for signs of a genetic disorder.
What happens during the procedure?
All that’s required for the test is a basic blood draw, typically from the arm but sometimes from another area of the body. Then the blood sample is taken to a laboratory for testing.
Is any special preparation needed?
No special preparation is needed for the test.
What are the risk factors?
There are slights risks of infection, bleeding, bruising or swelling related to the blood draw.
Reviewed by: Parul B Jayakar, MD
This page was last updated on: 8/22/2018 1:52:17 PM
From the Newsdesk
Nicklaus Children's Hospital will be one of a handful in the country to offer a fast turn-around on genome sequencing that can be a key to saving infants with rare and hard-to-diagnose genetic disorders. As seen on The Miami Herald.