Amniocentesis at Vardhan Fertility Centre
Accurate Prenatal Diagnosis to Ensure a Healthier Tomorrow
Amniocentesis is an advanced prenatal diagnostic test performed to detect genetic and chromosomal abnormalities in the developing baby. At Vardhan Fertility Centre, our fetal medicine experts perform this test with high precision and safety, offering expecting parents peace of mind through early, reliable information.
Amniocentesis is a procedure done between 15 to 20 weeks of pregnancy, where a small amount of amniotic fluid is withdrawn from the sac surrounding the baby using a thin needle under ultrasound guidance. This fluid contains fetal cells and proteins that can be tested for genetic conditions, chromosomal abnormalities, and certain infections.
- Down syndrome (Trisomy 21)
- Edwards syndrome (Trisomy 18)
- Neural tube defects (e.g., spina bifida)
- Sickle cell anemia and thalassemia
- Muscular dystrophy
- Certain metabolic disorders
- Fetal infections (if suspected)
- Women over age 35
- Abnormal findings on NT scan or anomaly scan
- Positive results from first-trimester screening or NIPT
- Family history of inherited genetic disorders
- Previous child with chromosomal/genetic conditions
- IVF pregnancies or those with multiple gestation concerns
- Slight chance of miscarriage (~0.1–0.3%)
- Minor cramping or spotting
- Temporary amniotic fluid leakage (rare)
- Highly experienced fetal medicine specialists
- Advanced ultrasound & sterile procedure rooms
- Genetic counseling before and after testing
- Close post-procedure monitoring
- Integration with full antenatal & maternity care
