Our Health Library information does not replace the advice of a doctor. Please be advised that this information is made available to assist our patients to learn more about their health. Our providers may not see and/or treat all topics found herein. Birth defects testing is done during pregnancy to look for possible problems with the baby (fetus). A birth defect may have only a minor impact on a child's life. Or it can have a major effect on quality or length of life. You and your doctor can choose from many tests. You may have no tests, one test, or many tests. You may have a screening test or a diagnostic test, or both. Screening tests show the chance that a baby has a certain birth defect or genetic condition, such as Down syndrome, spina bifida, or trisomy 18. Diagnostic tests show if a baby has a certain birth defect or genetic condition. The decision to test for birth defects is personal. There's a lot to think about, like what the results would mean to you and how they might affect your choices. If you choose testing, you may want to talk with a genetic counselor to discuss reasons to have or not have the test. Testing may be done during pregnancy to look for possible problems with the baby. Birth defects and genetic conditions include: There are two types of tests for birth defects and genetic conditions. A screening test can't tell you for sure that your baby has a problem. If you decide to have screening, you may have only first-trimester tests or only second-trimester tests. Or you may have an integrated screening test. This combines the results of first-trimester and second-trimester tests. Your doctor can tell you which tests are available and which ones might be best for you. It may not be easy to decide about testing for birth defects or genetic conditions. You may want to talk with a genetic counselor, who can discuss the reasons to have or not have a test. A counselor can also help you find other resources for support and decision-making. The decision to test for birth defects is personal. There's a lot to think about, like what the results would mean to you, and how they might affect your choices. Some birth defects—like a cleft palate or certain heart problems—can be fixed with surgery after birth. But other defects can't be fixed. If you choose to have a test, you may want to talk with a genetic counselor. The counselor can talk with you about the reasons to have or not have the test. They can also help you find other resources for support and decision-making. Here are some things to think about when deciding to test for birth defects. Here are some things to think about when deciding about early fetal ultrasound screening. Here are some things to think about when deciding to have a CVS test. Here are some things to think about when deciding to have an amniocentesis test. Current as of: April 30, 2024 Author: Ignite Healthwise, LLC Staff Current as of: April 30, 2024 Author: Ignite Healthwise, LLC Staff Clinical Review Board This information does not replace the advice of a doctor. Ignite Healthwise, LLC disclaims any warranty or liability for your use of this information. Your use of this information means that you agree to the Terms of Use and Privacy Policy. Learn how we develop our content. To learn more about Ignite Healthwise, LLC, visit webmdignite.com. © 2024 Ignite Healthwise, LLC. Healthwise, Healthwise for every health decision, and the Healthwise logo are trademarks of Ignite Healthwise, LLC.Birth Defects Testing
Condition Basics
What is birth defects testing?
What are the types of tests?
Should you have birth defects tests?
Types of Tests
Test When it's usually done What it involves First-trimester blood tests 10 to 13 weeks These tests measure the level of two substances in your blood that are related to certain genetic conditions: beta-hCG and PAPP-A. These blood tests and the nuchal translucency test are often done together and called first-trimester screening. These tests may be the first part of an integrated screening test. Nuchal translucency test 10 to 13 weeks This test uses ultrasound to measure an area at the back of the baby's neck. An increase in the thickness can be an early sign of certain genetic conditions, such as Down syndrome. Cell-free fetal DNA 10 weeks or later This test looks at the baby's DNA in your blood. It can help find genetic problems like Down syndrome or trisomy 18. This test is an option if you have risk factors for having a baby with certain genetic conditions. It's not used as a general screening test or if you are carrying twins. Alpha-fetoprotein (AFP) blood test 15 to 18 weeks This blood test screens for certain structural problems, such as neural tube defects, and certain chromosome problems, such as Down syndrome. Quad screen blood test (second trimester) 15 to 22 weeks This test checks the level of four substances in your blood that are related to certain birth defects and genetic conditions. They are beta-hCG, AFP, inhibin A, and a type of estrogen (estriol, or uE3). This is the second part of an integrated screening test. Fetal ultrasound 18 to 22 weeks This test produces an image of your developing baby. It can be used in the second trimester to find structural problems such as heart defects and neural tube defects. Test When it's usually done What it involves Chorionic villus sampling (CVS) 10 to 13 weeks (first trimester) A doctor takes a sample of cells from the placenta. The test can be used to find chromosome problems. These include Down syndrome and family diseases such as sickle cell disease or cystic fibrosis. It cannot find neural tube defects. Amniocentesis 15 to 20 weeks (second trimester) A doctor takes a sample of the amniotic fluid, which contains some of the baby's cells. This test can find chromosome problems as well as neural tube defects, such as spina bifida. Deciding About Testing
Birth defects testing
Early fetal ultrasound
Chorionic villus sampling (CVS)
Amniocentesis
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All Healthwise education is reviewed by a team that includes physicians, nurses, advanced practitioners, registered dieticians, and other healthcare professionals.
All Healthwise education is reviewed by a team that includes physicians, nurses, advanced practitioners, registered dieticians, and other healthcare professionals.
Our Health Library information does not replace the advice of a doctor. Please be advised that this information is made available to assist our patients to learn more about their health. Our providers may not see and/or treat all topics found herein. Current as of: April 30, 2024 Author: Ignite Healthwise, LLC Staff Clinical Review BoardBirth Defects Testing
All Healthwise education is reviewed by a team that includes physicians, nurses, advanced practitioners, registered dieticians, and other healthcare professionals.