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  2. Down syndrome - Wikipedia

    en.wikipedia.org/wiki/Down_syndrome

    Guidelines recommend screening for Down syndrome to be offered to all pregnant women, regardless of age. [ 111 ] [ 112 ] A number of tests are used, with varying levels of accuracy. They are typically used in combination to increase the detection rate. [ 29 ]

  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

    Screening for Down syndrome by a combination of maternal age and thickness of nuchal translucency in the fetus at 11–14 weeks of gestation was introduced in the 1990s. [7] This method identifies about 75% of affected fetuses while screening about 5% of pregnancies. Natural fetal loss after positive diagnosis at 12 weeks is about 30%. [6]

  5. Prenatal testing - Wikipedia

    en.wikipedia.org/wiki/Prenatal_testing

    Screening can detect problems such as neural tube defects, chromosome abnormalities, and gene mutations that would lead to genetic disorders and birth defects such as spina bifida, cleft palate, Down syndrome, trisomy 18, Tay–Sachs disease, sickle cell anemia, thalassemia, cystic fibrosis, muscular dystrophy, and fragile X syndrome.

  6. 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.

  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. Settings A-Z - AOL Help

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    Get answers to your AOL Mail, login, Desktop Gold, AOL app, password and subscription questions. Find the support options to contact customer care by email, chat, or phone number.

  9. Pappalysin-1 - Wikipedia

    en.wikipedia.org/wiki/Pappalysin-1

    For example, low PAPPA may be commonly seen in prenatal screening for Down syndrome. [2] Low levels may alternatively predict issues with the placenta, resulting in adverse complications such as intrauterine growth restriction, preeclampsia, placental abruption, premature birth, or fetal death. This enzyme catalyses the following chemical reaction: