How Early Can Blood Tests Reveal Baby’s Gender?

Are you interested in a DNA Gender Blood Test?

We are living in a world where we can get everything delivered to us the moment we want it. For example, we have movies, music, and shows, all of these can be delivered to us the moment we would like them. So, having to wait to find out the gender of your baby feels downright prehistoric.

However, you are in luck. Over the years, some pretty big strides have been made in the last few years which involve the timing and ease with which you can find out the gender of your unborn baby. How? With DNA Gender Blood Test.

But we are not at the, “hey, I ordered the gender of my baby, can I know within 30 minutes” point. However, improvements have been made with NIPTs.

When Should You See Your Doctor?

Before we get into the ways of finding out the gender of your baby, shouldn’t you first find out if you are pregnant with your doctor? If your home pregnancy test has given you a positive sign, it’s time you should sign an appointment with your OB-GYN.

When it comes to prenatal visits, you and your baby will be offered full support, which should be done once a month until the 28^th week of pregnancy. After this, the frequency should change to twice a month until you are 36 weeks pregnant.

Blood Tests You Can Have Done by Your Doctor

In the past, the standard of care for those at risk of having a baby with certain genetic conditions or other complications was one of two generic screenings performed in the first trimester: chorionic villus sampling or amniocentesis, according to Healthline.

A decade ago, innovative researchers introduced a significantly less intrusive method known as cell-free DNA screening for expectant parents. This revolutionary technique capitalizes on the fact that traces of your baby’s DNA are detectable in your blood. This advancement has paved the way for the screening of prevalent genetic fetal conditions, including:

• Down syndrome
• Edwards syndrome
• Patau syndrome

These conditions represent some of the most frequently encountered genetic anomalies in unborn babies.

How do Blood Tests Work?

During pregnancy, a small amount of the baby’s DNA circulates in the mother’s bloodstream. NIPTs leverage this fact to analyze the fetal DNA present in the mother’s blood. This DNA carries genetic information, including markers that can reveal the baby’s sex.

The procedure involves a blood draw from the mother, usually taken from a vein in her arm. Moreover, the blood sample is then sent to a laboratory, where advanced genetic testing techniques are used to analyze the DNA. Therefore, this analysis can accurately determine whether the baby is a boy or a girl based on the presence of Y-chromosomal DNA for a boy and its absence for a girl.