Amniocentesis
A definitive diagnostic test for genetic conditions
Amniocentesis is a prenatal test used to detect certain genetic and chromosomal conditions in a developing baby.
In this procedure, a small amount of amniotic fluid—surrounding the baby inside the uterus—is carefully extracted using a thin needle under ultrasound guidance.
This fluid contains fetal cells, which are then analyzed in a laboratory.
The test is usually performed between 15 to 20 weeks of pregnancy and is considered highly accurate (around 99%) in identifying conditions such as:
* Down syndrome
* Cystic fibrosis
* Neural tube defects
Duration
20–30 minutes (procedure) + observation time
Cost
₹8,000 – ₹20,000 (approximately)
Preparation:
Doctor consultation required; avoid heavy activity before/after; consent needed
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Medical Professionals
Meet the Health Experts Behind Your Care
Dr. Aviana Lexa
Dr. Eddie Shock
Dr. Whitney Kyle
Dr. Lawson Bourne
Dr. Hailey Marie
