Amniocentesis Testing
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What is Amniocentesis?
A prenatal test called amniocentesis is carried out in the second trimester, usually between weeks 15 and 20 of pregnancy. Using a fine needle, a tiny amount of amniotic fluid is extracted from the womb. Fetal cells and proteins found in this fluid offer crucial details regarding the genetic well-being of the unborn child.
Why is Amniocentesis Done?
This test is advised in some circumstances for the following:
Why is Amniocentesis Done?
Amniocentesis is done to obtain amniotic fluid for genetic or other testing, usually to detect chromosomal or genetic conditions in the baby.
What Does Amniocentesis Check?
Amniocentesis can check:
How is Amniocentesis Performed?
The procedure usually takes about 15–20 minutes:
Ultrasound locates the baby and the safest site for needle insertion.
A thin, sterile needle is passed through the abdomen into the amniotic sac.
A small amount of amniotic fluid is withdrawn and sent for analysis.
You may rest briefly; results are discussed with you after the lab completes testing.
How to Prepare for Amniocentesis
Usually performed after 15 weeks. Your doctor may advise a full or empty bladder. No routine fasting. Consent and counseling are done before the procedure.
Understanding Amniocentesis Results
Normal results suggest no chromosomal or tested genetic abnormality. Abnormal results indicate a condition; our team will explain implications, options, and follow-up. Amniocentesis is generally safe when performed by experienced specialists; our team minimizes risks and provides post-procedure care.
Cost of Amniocentesis
Cost of amniocentesis varies by center and tests performed. Contact us for pricing and to book an appointment.