DNM2 Gene Centronuclear Myopathy Type 1 NGS Genetic Test
Short Name: DNM2 CNM Type 1 NGS Test
Also known as: Autosomal Dominant Centronuclear Myopathy, CNM Type 1
DNM2 Gene Centronuclear Myopathy Type 1 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood, Extracted DNA, or FTA Card sample 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 identify mutations in the DNM2 gene that cause Centronuclear Myopathy Type 1, aiding in diagnosis and management.
- Test Code
- 1538
- Price
- ₹20,000
- Sample Type
- Blood, Extracted DNA, or FTA Card sample
- Result Time
- 3 to 4 weeks
- Fasting Required
- No
- Method
- NGS Technology
Sample Collection
No special preparation required. Ensure proper identification and informed consent.
Method: Venipuncture or Saliva collection
Laboratory Analysis
Sample collected via venipuncture or saliva method with minimal discomfort.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Keep sample at ambient room temperature.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the DNM2 gene that cause Centronuclear Myopathy Type 1, aiding in diagnosis and management.
How to Prepare
- Use sterile collection equipment
- Label samples correctly with patient details
- Transport samples at room temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for DNM2 mutations can confirm diagnosis and aid in genetic counseling for families affected by centronuclear myopathy."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Sample contaminated
- Improper storage or handling
Understanding Your Results
Positive
Pathogenic mutation detected; confirms diagnosis and supports genetic counseling
Negative
No pathogenic mutation detected; clinical correlation needed to rule out other causes
If symptoms of muscle weakness or wasting are present, or if there is a family history of centronuclear myopathy.
Limitations
- ⚠May not detect all types of mutations
- ⚠Results require clinical correlation
- ⚠Not a substitute for comprehensive clinical evaluation
Risks & Considerations
- ●Minor bruising at blood draw site
- ●Very low risk of infection
Interfering Factors
- ●Poor sample quality
- ●Contamination of DNA sample
- ●Hemolyzed blood sample
Compare With Similar Tests
| Test | DNM2 Gene Centronuclear Myopathy Type 1 NGS Genetic Test | MTM1 Gene Centronuclear Myopathy Test |
|---|---|---|
| Comparison | DNM2 Gene Centronuclear Myopathy Type 1 NGS Genetic Test |
Frequently Asked Questions
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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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