Birth Defects Testing - Topic Overview
What are birth defects tests?
Birth defects tests are done
during pregnancy to look for possible problems with the
baby (fetus). Birth defects develop when something is
wrong with genes or
chromosomes, an organ, or body chemistry. A birth
defect may have only a mild impact on a child's life, or it can have a major
effect on quality of life or life span.
What are the types of tests?
There are two types of birth
defects tests: screening and diagnostic.
- Screening tests show the chance that a baby has a certain birth defect. It can't tell you for sure that your baby has a problem. If the test
result is "positive," it means that your baby is more likely to have that birth
defect. So your doctor may want you to have a diagnostic test to make sure. If
the screening test result is "negative," it means that your baby probably
doesn't have that birth defect. But it doesn't guarantee that you will have a
normal pregnancy or baby.
- Diagnostic tests show if a baby has a certain birth defect.
Screening tests for birth defects are blood tests and ultrasounds. The blood tests are used to look for the amount of certain substances in your blood. The doctor uses an ultrasound to look for certain changes in the baby. Diagnostic tests involve taking some of the baby's cells to look at the genes and chromosomes.
No test is 100%
accurate. A test may be negative even when the baby has a birth
defect. This is called a
false-negative test result. It's also possible that a
test will be positive—meaning the test result is abnormal—but the baby does not
have the problem. This is called a
false-positive test result.
You may have only first-trimester tests or only second-trimester tests. Or you may have an integrated test. This test combines the results of tests you have in your first trimester and second trimesters.