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Test tube baby nt How about test tube baby NT test? When is it appropriate?



How about the test tube baby NT test?

Test tube baby NT (fetal nuchal transparent band) test is an advanced prenatal screening technology, which can assess whether the fetus has chromosome abnormalities and the risk of congenital heart disease. This article will elaborate on the test tube baby NT examination from four aspects.

 Test tube baby nt How about test tube baby NT test? When is it appropriate?

1. Principle of test tube baby NT examination

In vitro NT examination, the thickness of the zona pellucida in the neck of the fetus is measured by ultrasound to assess whether the fetus has chromosome abnormalities, especially the risk of Down syndrome. Normally, the zona pellucida of the neck of the fetus is thin. If the thickness of the zona pellucida of the neck exceeds the normal range, it may indicate that the fetus is at risk of chromosomal abnormalities.

NT examination is usually carried out at 12-14 weeks of pregnancy. Women who receive the examination need to undergo ultrasonic examination. The doctor will measure the thickness of the fetal nuchal translucency band and further assess the risk in combination with other indicators such as blood examination results.

2. Advantages of test tube baby NT examination

Test tube baby NT examination has the following advantages:

First of all, this examination is non-invasive, safe and reliable, and will not cause any harm to the fetus and mother. The risk assessment of fetal chromosomal abnormalities can be obtained by only one ultrasonic examination and blood examination.

Secondly, NT examination can be carried out at an early stage of pregnancy, providing opportunities for early screening. Early detection of chromosomal abnormalities helps couples make decisions and arrange further examinations. If the test results are abnormal, the doctor may suggest more accurate diagnostic tests such as amniocentesis.

Finally, NT examination can not only assess the risk of chromosomal abnormalities, but also preliminarily screen whether the fetus has the risk of congenital heart disease. This provides opportunities for early intervention and treatment.

3. Applicable population of test tube baby NT examination

Test tube baby NT examination is applicable to the following populations:

First, older pregnant women. With the growth of age, the risk of chromosomal abnormalities will also increase. NT examination can provide an opportunity for early screening.

Secondly, couples with a family history of chromosomal abnormalities. If someone in the couple carries a chromosome abnormality gene, NT examination can help determine whether the fetus is affected.

In addition, NT examination is also recommended in the case of fetuses with chromosomal abnormalities or pregnant women with other high-risk factors.

4. Significance of test tube infant NT examination

Test tube infant NT examination is of great significance to both couples and fetuses:

For couples, NT examination can provide them with valuable information to help them make decisions on whether to carry out further diagnosis or treatment. Couples can choose to continue pregnancy, make accurate diagnosis or terminate pregnancy according to the examination results and risk assessment.

For fetus, NT examination can provide an opportunity for early screening, which is helpful for early detection and intervention of chromosome abnormalities and congenital heart diseases. This will help improve the quality of life and health of infants.

Summary

Test tube infant NT examination is a non-invasive and safe prenatal screening technology, which can assess the risk of chromosomal abnormalities by measuring the thickness of the zona pellucida in the neck of the fetus. This examination has the advantages of early screening, safety and reliability, and is suitable for older pregnant women, couples with family history and other high-risk factors. NT examination is of great significance to couples and fetuses, providing them with decision-making basis, and helping to identify and deal with potential problems early, so as to improve the quality of life and health of fetuses.

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