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Doctor insights on: Ultrascreen Nuchal

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What is a nuchal scan?

What is a nuchal scan?

Nuchal Translucency : Nuchal Translucency is a screening test to determine risk of chromosome abnormalities in a fetus. When the NT is greater than 3.5 mm, there is a 1 in 5 chance of a chromosome abnormality such as Turner or Down syndrome, or Trisomy 18. Additional tests should be ordered by an OB or genetic counselor for confirmation. A mother may decide to continue or end of the pregnancy based on the information. ...Read more

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What is nuchal translucency?

What is nuchal translucency?

Nuchal Translucency : Nuchal Translucency is a screening test to determine risk of chromosome abnormalities in a fetus. When the NT is greater than 3.5 mm, there is a 1 in 5 chance of a chromosome abnormality such as Turner or Down syndrome, or Trisomy 18. Additional tests should be ordered by an OB or genetic counselor for confirmation. A mother may decide to continue or end of the pregnancy based on the information. ...Read more

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What is nuchal translucency for?

What is nuchal translucency for?

Nuchal Translucency : Nuchal Translucency is a screening test to determine risk of chromosome abnormalities in a fetus. When the NT is greater than 3.5 mm, there is a 1 in 5 chance of a chromosome abnormality such as Turner or Down syndrome, or Trisomy 18. Additional tests should be ordered by an OB or genetic counselor for confirmation. A mother may decide to continue or end of the pregnancy based on the information. ...Read more

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What is a nuchal translucency test?

What is a nuchal translucency test?

Nuchal Translucency : Nuchal Translucency is a screening test to determine risk of chromosome abnormalities in a fetus. When the NT is greater than 3.5 mm, there is a 1 in 5 chance of a chromosome abnormality such as Turner or Down syndrome, or Trisomy 18. Additional tests should be ordered by an OB or genetic counselor for confirmation. A mother may decide to continue or end of the pregnancy based on the information. ...Read more

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How do they measure nuchal translucency?

How do they measure nuchal translucency?

Ultrasound: Nuchal translucency (nt) is typically measured between weeks 11 and 14. The sonographer measures the thickness of the tissues of the back of the fetal neck. After the image is magnified, calipers are placed along the inner margin of the tissues of the neck. ...Read more

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Nuchal thickness 9.2mm in 28 wks is it down?

Nuchal thickness 9.2mm in 28 wks is it down?

Possible: A nuchal thickness of greater than 6 mm is associated with Down's syndrome. This is just a screening tool, however, and does not mean the baby has it. you need to talk with your OB about further testing. ...Read more

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Nuchal translucency scan at 4.4mm, what to do?

Nuchal translucency scan at 4.4mm, what to do?

Nuchal Translucency : Nuchal Translucency is a screening test to determine risk of chromosome abnormalities in a fetus. When the NT is greater than 3.5 mm, there is a 1 in 5 chance of a chromosome abnormality such as Turner or Down syndrome, or Trisomy 18. Additional tests should be ordered by an OB or genetic counselor for confirmation. A mother may decide to continue or end of the pregnancy based on the information. ...Read more

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Nuchal translucency scan at 4.4mm. What does this mean?

Nuchal translucency scan at 4.4mm. What does this mean?

Nuchal Translucency : Nuchal Translucency is a screening test to determine risk of chromosome abnormalities in a fetus. When the NT is greater than 3.5 mm, there is a 1 in 5 chance of a chromosome abnormality such as Turner or Down syndrome, or Trisomy 18. Additional tests should be ordered by an OB or genetic counselor for confirmation. A mother may decide to continue or end of the pregnancy based on the information. ...Read more

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Ultrasound showed thick nuchal foldworried. What does this mean?

Ultrasound showed thick nuchal foldworried. What does this mean?

Nuchal Translucency : Nuchal Translucency is a screening test to determine risk of chromosome abnormalities in a fetus. When the NT is greater than 3.5 mm, there is a 1 in 5 chance of a chromosome abnormality such as Turner or Down syndrome, or Trisomy 18. Additional tests should be ordered by an OB or genetic counselor for confirmation. A mother may decide to continue or end of the pregnancy based on the information. ...Read more