Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test
Short Name: Prenatal Panel 2 Amniotic Fluid
Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test test available at DNA Labs India for ₹5,850. Uses Two Dimensional Electrophoresis on Amniotic fluid samples. Results in Results are typically available within 10 days after sample receipt.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
This assay detects specific sulphate with qualitative analysis of their relative amounts, useful for diagnosing Mucopolysaccharidoses (MPS) and monitoring enzyme replacement therapy. It helps in early detection of genetic abnormalities, enabling informed prenatal management.
- Test Code
- 1393
- Price
- ₹5,850
- Sample Type
- Amniotic fluid
- Result Time
- Results are typically available within 10 days after sample receipt.
- Fasting Required
- No
- Method
- Two Dimensional Electrophoresis
Sample Collection
Sample should be taken after 16 weeks gestation. A duly filled Prenatal genetic testing consent form (Form 18) is mandatory. Sample to be dispatched with prior appointment.
Method: Amniocentesis
Laboratory Analysis
Amniocentesis procedure: A thin needle is inserted through the abdomen into the uterus to collect amniotic fluid under ultrasound guidance.
Report Delivery
Monitor for any discomfort or complications post-procedure. Results are typically available within 10 days.
Timeline: Results are typically available within 10 days after sample receipt.
Patient Instructions
About This Test
Who Should Get This Test
This assay detects specific sulphate with qualitative analysis of their relative amounts, useful for diagnosing Mucopolysaccharidoses (MPS) and monitoring enzyme replacement therapy. It helps in early detection of genetic abnormalities, enabling informed prenatal management.
How to Prepare
- Collect 10 mL (7 mL min.) of amniotic fluid in a sterile screw capped container.
- Ship at 18-22°C within 24 hours. DO NOT FREEZE.
- Ensure sample is taken after 16 weeks of gestation.
- Submit with completed Prenatal genetic testing consent form (Form 18).
- Arrange prior appointment for sample dispatch.
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for early detection of genetic conditions, allowing for informed decision-making and timely interventions during pregnancy."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
Understanding Your Results
Normal
No detectable genetic abnormalities. Continue routine prenatal care.
Abnormal
Genetic disorder detected. Consult with a genetic counselor and specialist for management options.
Inconclusive
Further testing recommended. Repeat test or use alternative methods.
Carrier Status
Parent is a carrier for a genetic condition. Genetic counseling advised for family planning.
If you have risk factors such as advanced maternal age, family history of genetic disorders, or abnormal prenatal screening results, consult your doctor about this test. After receiving results, seek genetic counseling for interpretation and next steps.
Risks & Considerations
- ●Minor risk of miscarriage (about 0.1-0.2%)
- ●Infection or bleeding at the needle site
- ●Amniotic fluid leakage
- ●Discomfort during procedure
Compare With Similar Tests
| Test | Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test | Chorionic Villus Sampling (CVS) | Non-Invasive Prenatal Testing (NIPT) | Maternal Serum Screening |
|---|---|---|---|---|
| Comparison | Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test | CVS is performed earlier (10-13 weeks) but carries slightly higher risk. Amniocentesis is done later with lower risk. | NIPT uses maternal blood and is non-invasive, but may have lower sensitivity for some disorders. | Blood test for markers, less invasive but may require confirmation with amniocentesis. |
Frequently Asked Questions
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