enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Down syndrome - Wikipedia

    en.wikipedia.org/wiki/Down_syndrome

    Trisomy 21. Down syndrome (also known by the karyotype 47,XX,+21 for females and 47,XY,+21 for males) [98] is mostly caused by a failure of the 21st chromosome to separate during egg or sperm development, known as nondisjunction. [91] As a result, a sperm or egg cell is produced with an extra copy of chromosome 21; this cell thus has 24 ...

  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. Nuchal scan - Wikipedia

    en.wikipedia.org/wiki/Nuchal_scan

    The results of all three factors may indicate a higher chance of Down Syndrome. If this is the case, the woman may be advised to have a more reliable screen such as cell-free fetal DNA screening or an invasive diagnostic test (such as chorionic villus sampling or amniocentesis).

  5. Prenatal testing - Wikipedia

    en.wikipedia.org/wiki/Prenatal_testing

    Meanwhile, of the 3792 women told they are low-risk by the Quad test, 2 of them will go on to deliver a baby with Down syndrome. The Quad test is therefore said to have a 4% positive predictive value (PPV) because only 4% of women who are told they are "high-risk" by the screening test actually have an affected fetus. The other 96% of the women ...

  6. Noninvasive prenatal testing - Wikipedia

    en.wikipedia.org/wiki/Noninvasive_prenatal_testing

    Noninvasive prenatal testing (NIPT) is a method used to determine the risk for the fetus being born with certain chromosomal abnormalities, such as trisomy 21, trisomy 18 and trisomy 13. [1][2][3] This testing analyzes small DNA fragments that circulate in the blood of a pregnant woman. [4] Unlike most DNA found in the nucleus of a cell, these ...

  7. Genetic testing - Wikipedia

    en.wikipedia.org/wiki/Genetic_testing

    As of 2015 it is the most sensitive and specific screening test for Down syndrome. [13] Newborn heel-prick blood sample collection Newborn screening – used just after birth to identify genetic disorders that can be treated early in life. A blood sample is collected with a heel prick from the newborn 24–48 hours after birth and sent to the ...

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

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

    For Ashley Zambelli, a surprise diagnosis allowed her to have an even more special bond with her children.. The Michigan-based mom, 23, recently found out she has Mosaic Down syndrome, a condition ...

  9. Inborn errors of metabolism - Wikipedia

    en.wikipedia.org/wiki/Inborn_errors_of_metabolism

    Because of the multiplicity of conditions, many different diagnostic tests are used for screening. An abnormal result is often followed by a subsequent "definitive test" to confirm the suspected diagnosis. [citation needed] Gas chromatography–mass spectrometry (GCMS) machine. Common screening tests used in the last sixty years: [citation needed]