Amniocentesis: What You Need to Know
Highlights In This Article Amniocentesis Overview Amniocentesis is a prenatal test performed after 15 weeks of pregnancy to detect genetic or chromosomal conditions. It is…
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Highlights In This Article Amniocentesis Overview Amniocentesis is a prenatal test performed after 15 weeks of pregnancy to detect genetic or chromosomal conditions. It is…
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Highlights In This Article Chorionic Villus Sampling (CVS) Chorionic villus sampling (CVS) is a prenatal diagnostic test performed during pregnancy. The test is conducted after…
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Highlights In This Article Nuchal Translucency Scan Overview A nuchal translucency scan is an ultrasound scan that measures the thickness of the space behind your…
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Highlights In This Article Down Syndrome Overview Down syndrome is a common genetic (chromosomal) condition that causes mild to moderate intellectual disability. People with Down…
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Highlights In This Article Understanding the Non-Invasive Prenatal Test (NIPT) The non-invasive prenatal test (NIPT) is a highly accurate screening test. Screening tests are used…
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Highlights In This Article Overview of Genetic Screening in Pregnancy Genetic screening, or prenatal screening, is available to anyone who is pregnant. These tests estimate…
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Highlights In This Article Morphology Scan A morphology (body part) scan is a routine prenatal test usually performed between 18 and 22 weeks of pregnancy….
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Highlights In This Article Carrier Status Screening Carrier status screening is a genetic test that identifies whether you carry genes for specific inherited health conditions….
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Highlights In This Article Genetic Counselling Genetic counselling is when you talk with a trained genetic counsellor about genetic conditions. Genetic counselling can help you:…
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