What Is an NT Scan in Pregnancy, and Why Is It Important? - #15244
I recently found out I’m pregnant, and my doctor recommended an NT scan in pregnancy during my first trimester. I had never heard of this test before, so I’m trying to understand why it’s necessary and what it detects. From what I’ve read, an NT scan (Nuchal Translucency scan) is performed between 11 to 14 weeks of pregnancy and helps assess the risk of chromosomal abnormalities like Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13). But how accurate is this test in detecting potential genetic issues? I also read that the NT scan measures the fluid at the back of the baby’s neck. If the fluid measurement is higher than normal, does that automatically mean there’s a problem, or could it just be a variation? What happens if the NT scan result is abnormal—are additional tests like NIPT (Non-Invasive Prenatal Testing) or amniocentesis necessary? Is there any way to naturally improve pregnancy health to reduce the risk of chromosomal abnormalities? Does Ayurveda recommend any dietary changes, herbal remedies, or prenatal care practices that support fetal development? If anyone has had an NT scan in pregnancy, what was your experience like? Did you have normal results, or did you need additional tests?
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