Pregnancy is a stage that can create doubts and confusion for the expecting couple. Especially with all the misinformation and myths floating on the internet, it can be difficult to separate accurate information from false narratives. 
 

In today's time, there are many tests and procedures available to safeguard the well-being of the mother and the unborn baby. A DNA test is among those widely relied upon by expectant mothers due to its many advantages. One of the common questions expectant mothers might have is if it is safe to perform a DNA test on an unborn child?

Let's briefly discuss the safety of DNA tests

Before further discussion, it is essential to learn about the two types of DNA tests. 

Invasive prenatal testing: Amniocentesis is one of the most popular invasive prenatal tests. In this method, a needle is inserted into the mother's womb to withdraw amniotic fluid from the amniotic sac surrounding the fetus.

Chorionic Villus Sampling (CVS) is another type of invasive prenatal testing, in which a sample of chorionic villi is taken from the placenta. Although generally considered safe, it is essential to understand there is always a risk, although very minimal, of miscarriage while going for invasive tests.

Non-invasive prenatal testing: Non-invasive prenatal testing is one of the safest types of DNA test on an unborn child. Since the DNA is acquired from the mother's blood using a prenatal DNA testing kit, there is no risk to the mother or unborn baby. Non-invasive prenatal DNA testing is helpful in detecting chromosomal abnormalities and the gender of the baby. You can get a conclusive result by conducting a NIPT test within 10 weeks of the pregnancy.
 

You can rely on the Prenatal Genetics Laboratory for performing safe DNA tests on the unborn child. Our lab boasts research specialists with knowledge and experience in DNA testing. Get in touch with us today to learn about everything we can do for you.