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Medical Conditions - Nuchal Translucency Scan

A nuchal translucency scan (NT scan) is a non-invasive prenatal test that uses ultrasound to measure the thickness of fluid at the back of a fetus's neck. This measurement can indicate an increased risk of chromosomal abnormalities such as Down syndrome, Edward syndrome, or Patau syndrome. The test is usually performed between 11 to 14 weeks of pregnancy and is often combined with a blood test to calculate the risk of fetal abnormalities. A high-risk result may prompt further testing, such as chorionic villus sampling (CVS) or amniocentesis, to confirm the diagnosis.

All nuchal translucency-scan Q&A

What should the nuchal fold measurement be at 20 weeks?

Hello, Welcome to icliniq.com. I understand your concern. A nuchal fold measurement of 4.9 mm is at the normal upper limit; however, a low-risk Non-invasive prenatal test (NIPT) is reassuring.

What do the double-marker laboratory test results suggest about the risk of trisomy?

Hello, Welcome to icliniq.com. I thoroughly read your query and understand your concern.

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What does the nuchal translucency scan indicate?

Hello, Welcome to icliniq.com. I understand your concern. A normal fetus's femur length should be more than the 5th percentile. This is not an actual nuchal translucency scan.

Why is nasal bone important in nuchal translucency scan?

Hi, Welcome to icliniq.com. Thank you for your query. I have gone through your reports (attachment removed to protect the patient's identity). Please send me her detailed ultrasound report here.

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