- Anjali Verma
Dr. Dolly Chavda provided exceptional care during my pregnancy. Her expertise in fetal medicine gave me peace of mind, and the entire team was incredibly supportive.
Overview
What is Chorionic Villus Sampling (CVS)?
CVS is a specialized prenatal diagnostic test performed between 11 to 13 weeks of pregnancy to detect chromosomal abnormalities and genetic disorders in the fetus. The test involves taking a small tissue sample from the placenta (chorionic villi), which shares the baby’s genetic makeup, allowing for early detection of conditions such as Down syndrome, cystic fibrosis, sickle cell disease, and other genetic disorders.
Why Choose
Why Choose Racham for CVS Testing?
At Racham Fetal Medicine Centre, Bengaluru, we are committed to providing:
Expert Fetal Medicine Specialists
Our specialists are highly trained in performing safe and accurate CVS procedures.
Comprehensive Genetic Screening
We test for a wide range of genetic and chromosomal abnormalities for early detection and informed decision-making.
Personalized Genetic Counseling
Our experts guide you through the process, explaining results and next steps clearly.
Trusted by Expecting Parents
Our reputation for excellence in fetal medicine makes us a preferred choice for prenatal genetic testing in Bengaluru.
Expert Fetal Medicine Specialists
Our specialists are highly trained in performing safe and accurate CVS procedures.
Comprehensive Genetic Screening
We test for a wide range of genetic and chromosomal abnormalities for early detection and informed decision-making.
Personalized Genetic Counseling
Our experts guide you through the process, explaining results and next steps clearly.
Trusted by Expecting Parents
Our reputation for excellence in fetal medicine makes us a preferred choice for prenatal genetic testing in Bengaluru.
Condition
Findings of Chorionic Villus Sampling (CVS) in Bengaluru
The CVS test provides crucial genetic insights about the developing baby. Key findings include:
Chromosomal Abnormalities Detection
- Down Syndrome (Trisomy 21): A genetic condition caused by an extra copy of chromosome 21, leading to developmental delays and intellectual disabilities.
- Edwards Syndrome (Trisomy 18): A rare but severe condition caused by an extra chromosome 18, resulting in serious developmental issues and a high risk of pregnancy loss.
- Patau Syndrome (Trisomy 13): A genetic disorder caused by an extra chromosome 13, associated with severe intellectual disabilities and physical abnormalities.
Inherited Genetic Disorders
- Cystic Fibrosis: A hereditary disorder affecting the lungs and digestive system, leading to thick mucus production and breathing difficulties.
- Sickle Cell Anemia: A blood disorder in which red blood cells become abnormally shaped, causing pain, anemia, and potential complications.
- Tay-Sachs Disease: A rare inherited condition that affects nerve cells in the brain and spinal cord, leading to severe neurological decline.
- Thalassemia: A blood disorder causing reduced hemoglobin production, leading to anemia and other complications.
Sex-Linked Disorders
- Duchenne Muscular Dystrophy: A genetic disorder affecting boys, leading to progressive muscle degeneration and weakness.
- Hemophilia: A bleeding disorder caused by mutations in the genes responsible for blood clotting, leading to excessive bleeding even from minor injuries.
- Complete Chromosomal Analysis: Provides a detailed study of fetal chromosomes to detect abnormalities such as deletions, duplications, or structural changes.
Why is the CVS Test Important?
Chorionic Villus Sampling (CVS) is a critical prenatal test for expecting parents who:
- Have a family history of genetic disorders.
- Received abnormal first-trimester screening results.
- Are at a higher risk of chromosomal abnormalities due to advanced maternal age (35+ years).
- Have previously had a baby with a genetic condition.
- Want early diagnostic confirmation rather than waiting for an amniocentesis at 15+ weeks.
Early detection allows for better medical planning and informed pregnancy decisions.
What Does the CVS Test Check For?
- During Chorionic Villus Sampling (CVS), our specialists examine:
Chromosomal Health – Detects chromosomal disorders such as Down syndrome, Turner syndrome, and Klinefelter syndrome. - Genetic Disease Markers – Identifies inherited genetic conditions like cystic fibrosis and sickle cell anemia.
- Sex Chromosomes – Determines fetal sex and identifies sex-linked disorders.
- Overall Genetic Structure – Provides a detailed chromosomal map of the fetus to detect any abnormalities.
Who Should Get a CVS Test?
Chorionic Villus Sampling (CVS) is recommended for women who:
✔ Have received abnormal NIPT (Non-Invasive Prenatal Test) or NT scan results.
✔ Have a history of chromosomal or genetic disorders in the family.
✔ Are 35 years or older, as the risk of chromosomal abnormalities increases with age.
✔ Had a previous pregnancy affected by a genetic disorder.
✔ Require definitive genetic testing for peace of mind.
At Racham Fetal Medicine Centre, Bengaluru, we provide comprehensive prenatal genetic counseling and testing for expecting parents seeking early clarity.
Free Online Consultation With Fetal Medicine Experts
Book AppointmentProcess
What Happens During the CVS Procedure?
The Chorionic Villus Sampling (CVS) test is a quick and minimally invasive procedure.
1
Preparation
A detailed ultrasound scan is performed to determine the placental position.
2
Sample Collection
A thin needle is inserted (through the abdomen or cervix) under ultrasound guidance to collect a small sample of placental tissue.
3
Laboratory Analysis
The DNA from the sample is analyzed to detect genetic conditions.
4
Results & Consultation
Results are typically available within 3 - 4 weeks, depending upon the type of genetic test performed.
Videos
Expert Care for Fetal Health
Informative ultrasound insights on fetal heart, brain, and pregnancy scans.
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Cardiac screening At anomaly scan
Fetal heart view in anomaly scan.
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Fetal Brain @ Anomaly scan
Ultrasound to check fetal brain development.
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Pregnancy ultrasound
Pregnancy ultrasound monitors fetal development
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Fetal Echo - Tetralogy of Fallot
Fetal Echo detects Tetralogy of Fallot in the fetus.
Gallery
Capturing Moments of Care & Hope
Visual insights into expert prenatal care and patient trust.
What Our Patients Say
Real experiences from patients on our specialized care.
Review us on
Google 
- Amita Rao
I’m grateful for the accurate diagnosis and treatment we received at Racham Fetal Medicine. Dr. Chavda’s professionalism and compassion were outstanding throughout the process.
- Priya Sharma
Thanks to Dr. Dolly, my high-risk pregnancy was managed flawlessly. The scans and advice were precise, and I felt confident every step of the way.
- Ritika Jain
We were impressed with the advanced diagnostics and the way the staff explained everything step by step. Thank you for making us feel so cared for!
Book an Appointment
Schedule Your Consultation at Racham Fetal Medicine Centre
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FAQ's
Frequently Asked Questions – Chorionic Villus Sampling (CVS)
Here are some commonly asked questions about the CVS to help you understand the process and benefits of this sampling test:
Yes, CVS is a safe and widely performed prenatal test. While there is a small risk of complications (such as miscarriage, less than 1%), it is performed under strict medical supervision to ensure safety.
CVS is usually done between 11 to 13 weeks of pregnancy, providing early and reliable genetic insights.
Some women experience mild discomfort or cramping, but the procedure is quick and well-tolerated. Local anesthesia is used when needed.
Results typically take 3-4 weeks, depending upon the type of genetic test performed.
The cost of CVS testing varies based on the medical facility and laboratory analysis. Contact Racham Fetal Medicine Centre for pricing and appointment details.
To schedule your Chorionic Villus Sampling (CVS) test at Racham Fetal Medicine Centre, Bengaluru, call us at +918095950077 or email rachamfetalmedicine@gmail.com to book an appointment online.
