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Amniocentesis is a procedure that lets doctors detect or rule out problems with your baby's health long before birth. In the uterus your baby is surrounded by amniotic fluid that provides protection and nourishment. Floating in the fluid are cells from your baby providing doctors with genetic material for testing. In amniocentesis, your doctor will take a sample of this fluid to test for specific genetic disorders and birth defects. Amniocentesis is usually done in the second trimester of pregnancy at 15 to 18 weeks. It is generally offered to women with certain risk factors: --age 35 or older which increases the risk of chromosomal disorders such as down syndrome. --a previous child or pregnancy with a birth defect --blood test or ultrasound suggesting a birth defect such as down syndrome or neural tube defects --or a family history of genetic disorders such as cystic fibrosis. Amniocentesis may also be done in the third trimester for these reasons: --to determine if the baby's lung...
