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  2. Nuchal scan - Wikipedia

    en.wikipedia.org/wiki/Nuchal_scan

    [12] In another study values of 79.6% and 2.7% for the combined screening were then improved with the addition of second trimester ultrasound scanning to 89.7% and 4.2% respectively. [13] A further study reported detection of 88% for trisomy 21 (Down syndrome) and 75% for trisomy 18 (Edwards syndrome), with a 3.3% false-positive rate. [14]

  3. Triple test - Wikipedia

    en.wikipedia.org/wiki/Triple_test

    The most common abnormality the test can screen is trisomy 21 (Down syndrome).In addition to Down syndrome, the triple and quadruple screens assess risk for fetal trisomy 18 also known as Edwards syndrome, open neural tube defects, and may also detect an increased risk of Turner syndrome, triploidy, trisomy 16 mosaicism, fetal death, Smith–Lemli–Opitz syndrome, and steroid sulfatase ...

  4. Obstetric ultrasonography - Wikipedia

    en.wikipedia.org/wiki/Obstetric_ultrasonography

    Although 91% of fetuses affected by Down syndrome exhibit this defect, 5% of fetuses flagged by the test do not have Down syndrome. Ultrasound may also detect fetal organ anomaly. Usually scans for this type of detection are done around 18 to 23 weeks of gestational age (called the "anatomy scan", "anomaly scan

  5. Everything you need to know about Down syndrome - AOL

    www.aol.com/news/everything-know-down-syndrome...

    Down Syndrome Symptoms Down syndrome is usually diagnosed during pregnancy through genetic screening or at birth through diagnostic tests. There are some distinct physical features that typically ...

  6. Prenatal testing - Wikipedia

    en.wikipedia.org/wiki/Prenatal_testing

    In fact, consider that Down syndrome affects about 1:400 pregnancies; if you screened 4000 pregnancies with a Quad test, there would probably be 10 Down syndrome pregnancies of which the Quad test, with its 80% sensitivity, would call 8 of them high-risk. The quad test would also tell 5% (~200) of the 3990 normal women that they are high-risk.

  7. Noninvasive prenatal testing - Wikipedia

    en.wikipedia.org/wiki/Noninvasive_prenatal_testing

    NIPT is used to detect an array of genetic disorders including Trisomy 13 (Patau Syndrome), Trisomy 18 (Edward's Syndrome), and Trisomy 21 (Down Syndrome). [32] It can also be used to determine the sex and paternity of a child while still in utero. The most common genetic condition tested for is Trisomy 21.

  8. A mom of 3 learned she had mosaic Down syndrome through ... - AOL

    www.aol.com/lifestyle/mom-3-learned-she-had...

    March 9, 2023 at 12:45 PM. A mom with mosaic Down syndrome chronicles her journey. (Photo: Getty Images) (Photo: Getty Images) ... “In the most common type of Down syndrome, there are 47 ...

  9. Echogenic intracardiac focus - Wikipedia

    en.wikipedia.org/wiki/Echogenic_intracardiac_focus

    Types of chromosome problems that are occasionally seen include trisomy 13 (Patau syndrome) or trisomy 21 (Down syndrome). [1] In the case of an isolated EIF, and no other ultrasound findings, some studies show that the risk for a chromosome abnormality is approximately two times a woman's background risk.