DRD2 Gene DYT11, DRD2 related NGS Genetic Test
Short Name: DRD2 Gene DYT11 NGS Test
Also known as: DRD2-related dystonia, DYT11 dystonia, DRD2 gene disorder
DRD2 Gene DYT11, DRD2 related NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood, Extracted DNA, or Blood on FTA Card samples. Results in 3 to 4 weeks. 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
To detect mutations in the DRD2 gene associated with DYT11 dystonia, enabling precise diagnosis and informed clinical management.
- Test Code
- 1577
- Price
- ₹20,000
- Sample Type
- Blood, Extracted DNA, or Blood on FTA Card
- Result Time
- 3 to 4 weeks
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No special preparation is required. Inform the healthcare provider about any medications or medical conditions.
Method: Venipuncture
Laboratory Analysis
A blood sample will be drawn from a vein in the arm by a trained phlebotomist.
Report Delivery
Apply pressure to the puncture site with a cotton ball to stop bleeding. Avoid strenuous activity with the arm for a few hours.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To detect mutations in the DRD2 gene associated with DYT11 dystonia, enabling precise diagnosis and informed clinical management.
How to Prepare
- Ensure patient identification
- Use aseptic technique
- Label sample correctly
- Transport to lab within stability period
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing with NGS technology provides comprehensive analysis for DRD2 gene disorders, aiding in early diagnosis and management."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Clotted blood sample
- Incorrect sample type
- Missing or mismatched identification
Understanding Your Results
Pathogenic Mutation Detected
Confirms diagnosis of DRD2 gene DYT11 disorder. Genetic counseling recommended.
Variant of Uncertain Significance (VUS)
Further testing or family studies may be needed.
No Pathogenic Variant Detected
DRD2 gene mutation not found. Consider other genetic or non-genetic causes.
If you experience symptoms such as involuntary movements, abnormal postures, or have a family history of dystonia, consult a neurologist or geneticist for evaluation.
Limitations
- ⚠May not detect large deletions or duplications
- ⚠Requires correlation with clinical findings
- ⚠Genetic counseling essential for interpretation
Risks & Considerations
- ●Minor bruising at the blood draw site
- ●Rare risk of infection
- ●No significant long-term risks
Interfering Factors
- ●Hemolyzed or lipemic blood samples
- ●Contaminated DNA extracts
- ●Improper sample storage
Frequently Asked Questions
What is DRD2 Gene DYT11?
What are the symptoms of DRD2 Gene DYT11?
How is DRD2 Gene DYT11 diagnosed?
What is the cost of the NGS Genetic Test?
Is home sample collection available?
How long does it take to get results?
Is genetic testing painful?
Can this test be done on children?
What does a positive result mean?
What if no mutation is detected?
Is genetic counseling provided?
How accurate is the NGS Genetic Test?
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We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
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