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  2. Amniocentesis - Wikipedia

    en.wikipedia.org/wiki/Amniocentesis

    An amniocentesis is typically performed in the second trimester between the 15th and 20th week of gestation. [5] Women who choose to have this test are primarily those at increased risk for genetic and chromosomal problems, in part because the test is invasive and carries a small risk of pregnancy loss . [ 5 ]

  3. Amniotic fluid - Wikipedia

    en.wikipedia.org/wiki/Amniotic_fluid

    Amniotic fluid is removed from the mother by an amniocentesis procedure, where a long needle is inserted through the abdomen into the amniotic sac, using ultrasound guidance such that the fetus is not harmed. Amniocentesis is a low risk procedure, with risk of pregnancy loss between 1 in 1,500 – 1 in 700 procedures.

  4. Prenatal testing - Wikipedia

    en.wikipedia.org/wiki/Prenatal_testing

    Amniocentesis: This can be done once enough amniotic fluid has developed to sample. Cells from the fetus will be floating in this fluid, and can be separated and tested. Miscarriage risk of amniocentesis is commonly quoted as 0.06% (1:1600). [68] By amniocentesis it is also possible to cryopreserve amniotic stem cells. [69] [70] [71] After 15 weeks

  5. Noninvasive prenatal testing - Wikipedia

    en.wikipedia.org/wiki/Noninvasive_prenatal_testing

    The use of ultrasound and biochemical markers to detect aneuploidies is usually done in the first and / or second trimester of pregnancy. [8] Aneuploidies is when a fetus retains an abnormal amount of haploid cells from their parents. However, both of these approaches have a high rate of false positive results of 2–7%. [9]

  6. Anomaly scan - Wikipedia

    en.wikipedia.org/wiki/Anomaly_scan

    Prior to 18 weeks' gestation, the fetal organs may be of insufficient size and development to allow for ultrasound evaluation. Scans performed beyond 22 weeks' gestation may limit the ability to seek pregnancy termination, depending on local legislation. [1] Two-dimensional (2D) is used to evaluate fetal structures, placenta, and amniotic fluid ...

  7. Confined placental mosaicism - Wikipedia

    en.wikipedia.org/wiki/Confined_placental_mosaicism

    CPM is diagnosed when some trisomic cells are detected on chorionic villus sampling and only normal cells are found on a subsequent prenatal test, such as amniocentesis or fetal blood sampling. In theory, CPM is when the trisomic cells are found only in the placenta.

  8. Chorionic villus sampling - Wikipedia

    en.wikipedia.org/wiki/Chorionic_villus_sampling

    CVS usually takes place at 10–12 weeks' gestation, earlier than amniocentesis or percutaneous umbilical cord blood sampling. It is the preferred technique before 15 weeks. [2] CVS was performed for the first time in Milan by Italian biologist Giuseppe Simoni, scientific director of Biocell Center, in 1983. [3]

  9. Rh factor testing - Wikipedia

    en.wikipedia.org/wiki/Rh_factor_testing

    Amniocentesis is another invasive procedure which can be used to collect fetal DNA samples. [medical citation needed] This procedure is usually done between the 15th and 20th week of pregnancy. The purpose of AMC is to extract a small amount of amniotic fluid as fetal cells may be shed from the fetus and are suspended in the amniotic fluid ...