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Genetic Screening in First Trimester Of Pregnancy - All You Need To Know

Why Is NT/NB Scan And Dual Marker Important In Pregnancy?

The nuchal translucency scan is an ultrasound that may detect the risk of a number of chromosomal abnormalities. A nuchal translucency scan is a part of the ultrasound scan that most pregnant women have at around 12 weeks of pregnancy. The result of a nuchal translucency scan may tell you if your baby has a high or low risk of a chromosomal abnormality , examples of chromosomal abnormalities include trisomy 21(down syndrome), trisomy 18 (Edward syndrome) or trisomy 13 (Patau syndrome).

Increased thickness of the nuchal translucency might indicate a chromosomal abnormality but it doesn’t tell you that your baby definitely has or doesn’t have an abnormality. The result will tell you if your baby is at high risk or low risk of chromosomal abnormalities in comparison to the general population.

The nuchal translucency scan is done between 11 to 14 weeks of pregnancy, usually the scan is done through abdomen.

The results of the nuchal translucency scan will not be used alone to calculate the risk of a chromosomal abnormality. All your first trimester screening is combined to calculate your risk. The calculation is based on the mothers age, nuchal translucency measurement of your baby, the gestational age of the baby, blood test and the baby nasal bone . Even if you are classified as high risk remember your baby probably doesn’t have a chromosomal abnormality. This is a screening test and further more increase diagnostic tests are available. Diagnostic tests will confirm about chromosomal abnormality. Read More: https://www.drshubhragoyal.com/welcome/blogs/genetic-screening-in-first-trimester-of-pregnancy

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