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  2. Prenatal testing - Wikipedia

    en.wikipedia.org/wiki/Prenatal_testing

    Uncertainty on genetic testing results from several reasons: the genetic test is associated with a disease but the prognosis and/or probability is unknown, the genetic test provides information different than the familiar disease they tested for, found genetic variants have unknown significance, and finally, results may not be associated with ...

  3. Noninvasive prenatal testing - Wikipedia

    en.wikipedia.org/wiki/Noninvasive_prenatal_testing

    If these tests indicate an increased risk of aneuploidy, then invasive diagnostic testing is used, such as amniocentesis or chorionic villus sampling. Many women, however, feel uncomfortable with the invasive testing, because of the risk associated with miscarriage, which is around 0.5%. [10]

  4. Genetic testing - Wikipedia

    en.wikipedia.org/wiki/Genetic_testing

    Genetic testing is often done as part of a genetic consultation and as of mid-2008 there were more than 1,200 clinically applicable genetic tests available. [23] Once a person decides to proceed with genetic testing, a medical geneticist, genetic counselor, primary care doctor, or specialist can order the test after obtaining informed consent .

  5. Chorionic villus sampling - Wikipedia

    en.wikipedia.org/wiki/Chorionic_villus_sampling

    Family history of a chromosomal abnormality or other genetic disorder; Parents are known carriers for a genetic disorder; Advanced maternal age (maternal age above 35). AMA is associated with increase risk of Down's syndrome and at age 35, risk is 1:400. [citation needed] Screening tests are usually carried out first before deciding if CVS ...

  6. Amniocentesis - Wikipedia

    en.wikipedia.org/wiki/Amniocentesis

    Transabdominal chorionic villus sampling is an alternative to amniocentesis if genetic diagnostic testing is to be performed in the first trimester between ten and 15 weeks' gestation. [3] It is important to note that prenatal genetic testing cannot identify all possible fetal genetic abnormalities or their outcomes. [5]

  7. Triple test - Wikipedia

    en.wikipedia.org/wiki/Triple_test

    The triple test, also called triple screen, the Kettering test or the Bart's test, is an investigation performed during pregnancy in the second trimester to classify a patient as either high-risk or low-risk for chromosomal abnormalities (and neural tube defects). The term "multiple-marker screening test" is sometimes used instead.

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  9. Pregnancy test - Wikipedia

    en.wikipedia.org/wiki/Pregnancy_test

    Immunologic pregnancy tests were introduced in 1960 when Wide and Gemzell presented a test based on in-vitro hemagglutination inhibition. This was a first step away from in-vivo pregnancy testing [40] [41] and initiated a series of improvements in pregnancy testing leading to the contemporary at-home testing. [41]