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  2. Prenatal testing - Wikipedia

    en.wikipedia.org/wiki/Prenatal_testing

    At early presentation of pregnancy at around 6 weeks, early dating ultrasound scan may be offered to help confirm the gestational age of the embryo and check for a single or twin pregnancy, but such a scan is unable to detect common abnormalities. Details of prenatal screening and testing options may be provided.

  3. 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.

  4. Chorionic villus sampling - Wikipedia

    en.wikipedia.org/wiki/Chorionic_villus_sampling

    It entails sampling of the chorionic villus (placental tissue) and testing it for chromosomal abnormalities, usually with FISH or PCR. 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]

  5. A week-by-week guide to common pregnancy symptoms - AOL

    www.aol.com/news/week-week-guide-common...

    Pregnancy Symptoms Week 1. It's a bit of a mind-bender, but you aren't actually pregnant during what doctors call "week one" of pregnancy. Instead, week one starts on the first day of your last ...

  6. Confined placental mosaicism - Wikipedia

    en.wikipedia.org/wiki/Confined_placental_mosaicism

    Specific chromosomes: The influence of CPM on fetal growth is chromosome specific. Certain chromosomes carry imprinted genes involved in growth or placental function, which may contribute to impaired pregnancy progress when CPM is detected. [7] Different chromosomes are observed at different frequencies depending on the type of CPM observed. [2]

  7. Amniocentesis - Wikipedia

    en.wikipedia.org/wiki/Amniocentesis

    Abnormal results from FISH studies should be confirmed with other cytogenetic testing, as false positives and negatives are possible [5] Karyotypes are another common test performed on amniotic fluid to visualize chromosome number and characteristics, with a result turnaround of up to three weeks. [1] Another test that may be performed is a ...

  8. Noninvasive prenatal testing - Wikipedia

    en.wikipedia.org/wiki/Noninvasive_prenatal_testing

    Aneuploidies are disorders in which a fetus has the incorrect number of chromosomes, either too many or not enough. [7] 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 ...

  9. Nuchal scan - Wikipedia

    en.wikipedia.org/wiki/Nuchal_scan

    As nuchal translucency size increases, the chances of a chromosomal abnormality and mortality increase; 65% of the largest translucencies (>6.5mm) are due to chromosomal abnormality, while fatality is 19% at this size. [2] A nuchal scan may also help confirm both the accuracy of the pregnancy dates and the fetal viability.

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