MT-ATP8 Gene Cardiomyopathy, apical hypertrophic, and neuropathy, MT-ATP8 related NGS Genetic Test
Short Name: MT-ATP8 NGS Test
Also known as: MT-ATP8 Gene Test, Cardiomyopathy Genetic Test, Neuropathy Genetic Test
MT-ATP8 Gene Cardiomyopathy, apical hypertrophic, and neuropathy, MT-ATP8 related NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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 SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
To detect mutations in the MT-ATP8 gene associated with cardiomyopathy, apical hypertrophic, and neuropathy for accurate diagnosis and management.
- Test Code
- 5198
- 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
- NGS Technology
Sample Collection
No special preparation required. Provide clinical history and undergo genetic counseling.
Method: Blood Draw
Laboratory Analysis
Blood sample will be drawn by a trained phlebotomist using sterile equipment.
Report Delivery
Apply pressure to the puncture site to stop bleeding and avoid strenuous activity.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To detect mutations in the MT-ATP8 gene associated with cardiomyopathy, apical hypertrophic, and neuropathy for accurate diagnosis and management.
How to Prepare
- Ensure proper patient identification
- Use sterile collection tubes
- Label samples correctly
- Transport samples at appropriate temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Early genetic testing for MT-ATP8 mutations can guide treatment and family planning for affected individuals."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed samples
- Insufficient sample volume
- Improper labeling or contamination
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of MT-ATP8 related disorder; clinical management and genetic counseling recommended.
No pathogenic variant detected
Unlikely to have MT-ATP8 related disorder; consider other genetic or non-genetic causes.
If symptoms persist, worsen, or if there is a family history of genetic disorders, consult a geneticist or cardiologist.
Limitations
- ⚠Test only detects known mutations in MT-ATP8 gene
- ⚠May not identify all genetic causes of symptoms
- ⚠Results require clinical correlation
Risks & Considerations
- ●Minimal risk from blood draw such as bruising or infection
- ●Emotional impact of genetic results on patient and family
Interfering Factors
- ●Sample degradation
- ●Contamination during collection or processing
Compare With Similar Tests
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| Comparison | MT-ATP8 Gene Cardiomyopathy, apical hypertrophic, and neuropathy, MT-ATP8 related NGS Genetic Test |
Frequently Asked Questions
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₹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.
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