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Pronounced: am-KNEE-o-sen-TEE-sisEn Español (Spanish Version)
Amniotic fluid surrounds the baby during pregnancy. Amniocentesis is the removal of a small amount of this fluid for testing.
Amniocentesis is most often done to see if there is an abnormality in your baby's genes (DNA). It can also be done to see if your baby is developing correctly.
Factors that indicate that you may need this procedure include:
- Age: over 35 years at the time of delivery
- Family history of chromosome abnormality
- Family history of inherited disorder
- Family history of neural tube defect (problems in spine and brain growth, such as spina bifida or anencephaly)
- Abnormal results from an earlier blood screening test, such as maternal serum alpha-fetoprotein (AFP)
Depending on your risk factors, cells in the amniotic fluid are tested for:
- Chromosome abnormalities. The results are usually ready within 14 days. Missing or extra chromosomes lead to physical birth defects and intellectual disability. Down's syndrome is one example.
- Inherited genetic diseases—Test results are usually ready in 1-5 weeks. Examples include:
Amniocentesis may also be done:
- To determine whether the baby's lungs are mature
- In high-risk pregnancies that may require early delivery
Last reviewedOctober 2012by Andrea Chisholm
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.