Pregnancy is a special journey - but it also brings questions and concerns about your baby's health. If you or your doctor suspect a risk of genetic or chromosomal conditions, Chorionic Villus Sampling (CVS) or Amniocentesis can help you get clear answers early in pregnancy.
At our advanced prenatal testing centre in Pune, we provide safe, precise, and compassionate prenatal diagnostic tests under expert supervision. We use ultrasound-guided techniques and modern lab testing to detect conditions like Down syndrome, thalassaemia, and cystic fibrosis with high accuracy.
Types of CVS & Amniocentesis Tests
Chorionic Villus Sampling (CVS)
Performed at 11-14 weeks to detect genetic and chromosomal conditions early.
Transcervical CVS
Sample taken through the cervix via thin catheter under ultrasound guidance.
Transabdominal CVS
Sample taken through the abdomen using a fine needle-€”minimal discomfort.
Amniocentesis (15-€“20 wks)
Analyzes amniotic fluid to assess chromosomal issues and neural tube defects.
Ultrasound-Guided
Real-time guidance improves accuracy and reduces risks during both procedures.
What It Detects
Down syndrome, Tay-Sachs, Thalassemia; amnio also detects spina bifida.
Safety & Risks
Low miscarriage risk (~0.2%). Sterile, ultrasound-guided techniques used.
Results & Counseling
Obstetrician/genetic counselor explains results and next steps with privacy.
Why Choose Our Clinic for CVS & Amniocentesis?
Expert Team: Obstetricians & genetic specialists experienced with high-risk and twin pregnancies.
Advanced Imaging: Real-time ultrasound guidance for safety and precision.
Certified Labs: Accurate, reliable genetic and chromosomal analysis.
Personalized Care: Pre-test counseling, clear result explanation, and ongoing support.
Confidential: Complete privacy and sensitive handling of medical information.
Peace of Mind: Early, accurate answers to help you plan a healthy pregnancy.
Who Performs These Tests?
Obstetrician/Gynecologist (OBGYN)
Performs CVS/Amniocentesis with ultrasound support and trimester-wise monitoring.
Fetal Medicine Specialist
Advanced expertise for high-risk cases; precise targeting and comprehensive follow-up.
Genetic Counselor
Explains reports, clarifies options, and supports informed decision-making.
Nutrition & Lifestyle Experts
Diet and supplement guidance to support healthy maternal outcomes.
Frequently Asked Questions (FAQs)
CVS is a prenatal diagnostic test performed at 11-€“14 weeks that collects a small placental tissue sample to detect genetic and chromosomal disorders such as Down syndrome, Tay-Sachs, and Thalassemia.
Amniocentesis is done at 15-€“20 weeks to analyze amniotic fluid for chromosomal and neural tube defects (e.g., spina bifida) and inherited disorders, providing detailed information for pregnancy management.
Your obstetrician or genetic counselor explains the results, discusses further testing if needed, and guides you through safe, informed next steps.
Typically recommended between 15-€“20 weeks, especially with abnormal screening results, family history of genetic disorders, or maternal age 35+.
When performed by experienced specialists, both tests are considered safe. Risks like miscarriage are rare (~0.2%). We use sterile, ultrasound-guided procedures to minimize risks.
No. CVS detects genetic/chromosomal disorders but not structural defects (e.g., spina bifida). For a complete assessment, your doctor may recommend detailed ultrasound or amniocentesis.