Amniocentesis

Amniocentesis is typically indicated for various reasons during pregnancy, such as abnormal ultrasound findings, positive screening test results, family history of genetic disorders, or previous pregnancy with chromosomal abnormalities.

The procedure involves inserting a thin needle through the abdomen into the amniotic sac to collect a small amount of amniotic fluid, which contains fetal cells. These cells are then analyzed for genetic abnormalities and chromosomal disorders.

Results usually take about 1-3 weeks and can provide information about the baby’s health, genetic makeup, and any potential risks or abnormalities. It’s important to discuss the potential risks and benefits of amniocentesis with a fetal medicine specialist before undergoing the procedure.