Boy or Girl

Genetic testing to tell if boy or girl

Medically acknowledged tests are considered the surest way to know if you are having a boy or a girl.

If your doctor has you in for genetic testing early in your pregnancy, he or she will probably also be able to tell the baby’s sex within the results. Keep in mind doctors do not perform this tests normally. She or he would only risk this type of test if your history or family history determines that there is a need for it. These tests are nearly 99% accurate in telling you the baby’s sex.

There are 2 different genetic test you could take: amniocentesis or chorionic villus sampling (CVS).

Amniocentesis

Amniocentesis is generally done after week 14. This test can be used to determine if your baby has a chromosomal disorder or for fetal lung maturity. The doctor would insert a needle through your belly and into the placenta to withdraw fluid. An ultrasound is used at the same time to guide the needle and keep it away from the baby.

Chorionic Villus Sampling (CVS)

CVS can be a done between the 8-10th week. This test is only for determining if your baby has a chromosomal disorder. The doctor places a small needle is placed either through the abdomen or through the vagina near the uterus to collect a small sample. Here an ultrasound is used to guide the needler away from the baby.

© 2008 The First Trimester.