DRD2 Gene Myoclonic dystonia, DRD2 related NGS Genetic Test
Short Name: DRD2 Gene Myoclonic Dystonia Test
Also known as: Myoclonus-dystonia syndrome, DRD2-related dystonia
DRD2 Gene Myoclonic dystonia, DRD2 related NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
To confirm the presence of DRD2 gene mutations in individuals suspected of having myoclonic dystonia, enabling early diagnosis and appropriate treatment planning.
- Test Code
- 1741
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 Weeks
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
Genetic counseling recommended to discuss implications and family history.
Method: Venipuncture
Laboratory Analysis
Blood sample collected via venipuncture.
Report Delivery
Sample processed for DNA extraction and NGS analysis.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To confirm the presence of DRD2 gene mutations in individuals suspected of having myoclonic dystonia, enabling early diagnosis and appropriate treatment planning.
How to Prepare
- Provide detailed clinical history
- Undergo genetic counseling session
- Ensure sample collection in sterile conditions
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Early genetic testing for DRD2 mutations is crucial for timely intervention and management of myoclonic dystonia symptoms."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed sample
- Insufficient sample volume
- Contaminated sample
Understanding Your Results
If symptoms such as jerky movements, tremors, or muscle stiffness are present, or if there is a family history of myoclonic dystonia.
Limitations
- ⚠Test is specific to DRD2 gene; other genetic causes may not be identified
- ⚠Results require clinical correlation
Risks & Considerations
- ●Minimal risk from blood draw
- ●Potential psychological impact of results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA quality
Frequently Asked Questions
What is the DRD2 Gene Myoclonic Dystonia NGS Genetic Test?
Who should consider this test?
What is the cost of the test in India?
How is the test performed?
Is home sample collection available?
How long does it take to get the results?
What does a positive result mean?
What are the treatment options for myoclonic dystonia?
Is genetic counseling required before the test?
Are there any risks associated with the test?
How accurate is the NGS genetic test?
Can this test detect other types of dystonia?
Related Tests
MERRF (Myoclonic Epilepsy Associated with Ragged Red Fibres) Mutation Detection Test
₹16,000Myotonic Dystrophy Comprehensive Profile Test
₹11,000MYF6 Gene Centronuclear Myopathy Type 3 NGS Genetic Test
₹20,000DRPLA (Dentatorubral-Pallidoluysian Atrophy) Gene Analysis Test
₹7,500KIF7 Gene Acrocallosal Syndrome NGS Genetic Test
₹20,000APTX Gene Ataxia-Oculomotor Apraxia Type 1 NGS Genetic Test
₹20,000Reference Laboratory Services
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.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
Book Your Test
Enter your details and we'll connect you within 15 minutes.