Amniocentesis: Things That You Should Know
During pregnancy, your baby may have a genetic disease. But thanks to the advancement in the medical field, there is a common test method used to determine this disease. This method is called the Amniocentesis. It is one of the prenatal tests used during pregnancy. Thanks to this test, you can learn about the genetic diseases in your baby. In this way, you can learn the precautions you can take before your baby is born. You can also start the treatment of possible diseases.
This test is used to learn more about the health and development of the unborn baby. For example, this test can be used to reveal whether the unborn baby has a genetic disease such as Down syndrome.
You should know that amniocentesis, not all risks for your baby and pregnancy are known. It can not detect all birth defects. Heart problems and structural problems such as cleft lip cannot be detected by amniocentesis. To find out about such problems, one should use another way, ultrasound. But if the parents have a significant genetic risk, it can detect the following conditions:
Amniocentesis poses a small risk for both mother and
baby. For this reason, the doctors usually apply this prenatal test to women
who are at significant risk for genetic diseases.
A few examples of significant risks:
After having this test, you should spend the rest of the day resting. It is very important that you do not lift heavy or have sexual intercourse for the next 2-3 days. It’s normal to have mild cramps over the next few days. You shouldn’t worry. However, if you have painful cramps, vaginal bleeding, or high fever, you should contact your doctor immediately.