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DNA Labs India

MT-TD Gene Mitochondrial myopathy, isolated NGS Genetic Test

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MT-TD Gene Mitochondrial myopathy, isolated NGS Genetic Test

Short Name: MT-TD Gene Mitochondrial Myopathy Test

Also known as: MT-TD Gene Mutation Test, Mitochondrial Myopathy Genetic Test, MT-TD NGS Test

MT-TD Gene Mitochondrial myopathy, isolated 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 3-4 weeks. Free home collection in 300+ cities across India.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect pathogenic mutations in the MT-TD gene associated with mitochondrial myopathy, aiding in diagnosis, treatment planning, and genetic counseling.

Test Code
5271
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3-4 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Provide clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of affected family members.

Method: Venipuncture

Step 2

Laboratory Analysis

Standard blood draw procedure using sterile technique.

Step 3

Report Delivery

Sample is processed for DNA extraction and next-generation sequencing analysis.

Timeline: 3-4 weeks

Patient Instructions

1
Before the Test:Genetic counseling and informed consent are required before sample collection.
2
During the Test:Blood sample is collected via venipuncture.
3
After the Test:Wait for 3-4 weeks for results and attend follow-up counseling for interpretation.

About This Test

Who Should Get This Test

To detect pathogenic mutations in the MT-TD gene associated with mitochondrial myopathy, aiding in diagnosis, treatment planning, and genetic counseling.

How to Prepare

  • Ensure proper patient identification
  • Use sterile collection tubes
  • Label samples correctly
  • Transport samples at recommended temperature

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Genetic testing is essential for diagnosing mitochondrial myopathy, guiding treatment, and providing family counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs required
ContainerEDTA tube or FTA card
Collection MethodVenipuncture

Sample Stability

Blood samples stable for 48 hours at 2-8°C
Extracted DNA stable for longer periods at -20°C
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Improper labeling or documentation

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the MT-TD gene, which are associated with mitochondrial myopathy.
Positive result: Pathogenic variant detected, confirming genetic predisposition to mitochondrial myopathy.
Negative result: No pathogenic variants detected, but clinical correlation is advised.
Variant of uncertain significance: Further testing or family studies may be recommended.
⚠️ When to Consult a Doctor:

Consult a geneticist or neurologist if symptoms persist, worsen, or if there is a family history of mitochondrial disorders.

Limitations

  • May not detect all genetic variants
  • Requires interpretation by a genetic counselor
  • Results may have variants of uncertain significance

Risks & Considerations

  • Minimal risk from blood draw (e.g., bruising, infection)
  • Psychological impact of genetic results

Interfering Factors

  • Sample degradation
  • Contamination
  • Technical errors in sequencing

Compare With Similar Tests

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Frequently Asked Questions

What is the MT-TD Gene Mitochondrial Myopathy Test?
It is a genetic test using next-generation sequencing to detect mutations in the MT-TD gene associated with mitochondrial myopathy.
What are the symptoms of MT-TD gene mitochondrial myopathy?
Symptoms include muscle weakness, exercise intolerance, vision or hearing problems, seizures, and cardiac abnormalities.
How is the test performed?
A blood sample is collected and analyzed using NGS technology to identify genetic variants.
What is the cost of the test?
The test costs INR 20,000, which includes genetic counseling and follow-up.
Is home sample collection available?
Yes, free home collection is available for online bookings across India.
How long does it take to get results?
Results are typically available in 3-4 weeks.
What sample type is required?
Blood, extracted DNA, or one drop of blood on an FTA card.
Is fasting required before the test?
No, fasting is not required.
Who should consider this test?
Individuals with symptoms of mitochondrial myopathy or a family history of the disorder.
What do the results mean?
Results indicate the presence or absence of pathogenic variants in the MT-TD gene, aiding diagnosis.
Is genetic counseling included?
Yes, the test cost includes genetic counseling and follow-up appointments.
Are there any risks associated with the test?
Risks are minimal, primarily related to blood draw, but psychological impact of results should be considered.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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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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