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4 Ways to Know Gender scan of the Baby in the womb

Many people rely on a Kønsscanning to find out the sex of the baby in the womb of a pregnant woman. Reporting to WebMD, some say that pregnant women who eat a lot during pregnancy are pregnant with a boy. There are also those who say that the fetal heart rate is more than 140 beats per minute (bpm) meaning that the mother is pregnant with a girl.

Another opinion says that pregnant women who experience severe nausea (morning sickness) throughout the day are a sign that they are pregnant with a baby girl. Unfortunately, until now there has been no research or study that proves the truth of this argument. But don’t worry, couples who want to know the sex of the baby in the womb can now take advantage of various medical technologies.

Launching Healthline, here are some ways to find out the sex of the baby according to the stage of pregnancy of the pregnant woman:

1. Ultrasonography (USG) test

The most common way to find out the sex of the baby during pregnancy is through an ultrasound examination. Ultrasound is a routine pregnancy test that uses sound waves. This test is not specifically used to determine the sex of the baby. More than that, this examination is useful for monitoring the development and overall health of the baby. Most doctors schedule an ultrasound between 18 weeks and 21 weeks of pregnancy. However, the sex of the baby can be seen by ultrasound at 14 weeks of gestation. However, the prediction of the baby’s sex by ultrasound is not always accurate. The reason is, sometimes the baby’s position does not fit or the genitals are not clear. Thus, the resulting conclusions may be wrong.

2. Non-invasive prenatal blood test Illustration of a pregnant woman.

One way to find out the sex of a baby without an ultrasound in the womb is a non-invasive prenatal blood test (NIPT). Like ultrasound, NIPT is actually not a special test to find out the sex of the baby in the womb. This test is mainly used to see whether or not there is a chromosomal abnormality such as Down syndrome. If the results are abnormal, the doctor will recommend further tests. This test can be done at the age of 10 months of pregnancy. Not only detecting chromosomal abnormalities, but this test can also determine the sex of the baby. Pregnant women can undergo this test when the gestational age enters 10 weeks. This test is done by taking a blood sample to detect the presence or absence of fetal DNA associated with chromosomal abnormalities. Because it also monitors chromosomes, this test can also be used to accurately determine the sex of the baby in the womb. This blood test is recommended for pregnant women over the age of 35, or who have given birth to a baby with a chromosomal abnormality.

3. Chronic villus sampling (CVS) genetic test

The chronic villus sampling (CVS) test is a genetic test used to identify Down syndrome or other genetic disorders. Besides being able to provide information on the baby’s genes in the womb, this test can also accurately reveal the sex of the baby. This test tests a sample of the chorionic villus or the type of tissue present in the placenta. How to find out the sex of the baby and genetic disorders with this test can be done at 10 weeks or 12 weeks of gestation. Doctors generally recommend that pregnant women undergo CVS examination if they are over the age of 35 and have a family history of chromosomal abnormalities. However, CVS genetic testing is not without risks. Some pregnant women experience cramps, bleeding, leakage of amniotic fluid, and are more at risk for premature labor. Consult a doctor to minimize the risk of side effects associated with CVS testing.

4. Amniocentesis test or known as amnio test is a test that helps to detect abnormalities in the fetus.

This test can also be used to determine the sex of the baby in the womb between 15 weeks and 18 weeks of gestation. The amnio test only takes about 30 minutes. The doctor will take a sample of the amniotic fluid. These cells will be tested to detect abnormalities such as Down syndrome, spina bifida, or other genetic disorders. Health care providers generally recommend an amnio test if the ultrasound results indicate an abnormality. Pregnant women aged over 35 years or who have a family history of chromosomal abnormalities are also advised to undergo an amnio test. Like the CVS genetic test, the amnio test.

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