What exactly is amniocentesis? | Gynaecologist in Borivali | Dr. Deepika Doshi

Amniocentesis is a pregnancy test used to identify genetic abnormalities, birth deformities, and other issues in an unborn baby. Typically, the test is performed between weeks 15 and 20 of pregnancy.

Amniocentesis is the examination of a sample of amniotic fluid. Amniotic fluid is a transparent or light yellow liquid that surrounds and protects a developing infant during pregnancy. The fluid includes cells that offer vital information about the health of your unborn baby.

Amniocentesis is a diagnostic test. That means it will tell you whether your baby has a specific health problem, and the results are almost always accurate. Prenatal screening methods for genetic diseases vary from diagnostic examinations. Prenatal screening tests have no risks for you or your baby, but they don't diagnose problems. They can only indicate whether or not your baby has a medical concern. If a screening test shows your baby could have a problem, your health care provider may recommend amniocentesis or another diagnostic test to find out the abnormalities

Amniotic fluid analysis is another term for it.

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