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COX15 Gene Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency type 2 NGS Genetic Test

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COX15 Gene Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency type 2 NGS Genetic Test

Short Name: COX15 Cardioencephalomyopathy NGS Test

Also known as: COX15 deficiency, Cytochrome c oxidase deficiency type 2, Fatal infantile cardioencephalomyopathy

COX15 Gene Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency type 2 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.

NGS Genetic TestInfants and Children🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

To diagnose COX15 Gene Cardioencephalomyopathy through genetic analysis.

Test Code
2514
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
Step 1

Sample Collection

No specific preparation required.

Method: Venipuncture or FTA Card

Step 2

Laboratory Analysis

Blood sample will be collected via venipuncture or FTA card.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling recommended before testing.
2
During the Test:Sample collection and analysis.
3
After the Test:Report delivery and genetic counseling for results.

About This Test

Who Should Get This Test

To diagnose COX15 Gene Cardioencephalomyopathy through genetic analysis.

How to Prepare

  • Ensure proper identification
  • Use sterile equipment

Doctor's Notes

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

"Early genetic testing is crucial for diagnosis and management of COX15-related disorders."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture or FTA Card

Sample Stability

Blood samples stable for 24 hours at room temperature
FTA cards stable for longer periods
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient sample volume

Understanding Your Results

Genetic testing for COX15 mutations helps in diagnosing cardioencephalomyopathy.
📊

Mutation Detected

Diagnosis of COX15 Gene Cardioencephalomyopathy confirmed

📊

No Mutation Detected

Disease unlikely, but clinical correlation recommended

⚠️ When to Consult a Doctor:

If symptoms such as developmental delays, seizures, or muscle weakness are present in infants.

Limitations

  • ⚠Test may not detect all mutations
  • ⚠Requires genetic counseling for interpretation

Risks & Considerations

  • ●Minimal risk from blood draw
  • ●Psychological impact of genetic diagnosis

Compare With Similar Tests

TestCOX15 Gene Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency type 2 NGS Genetic TestMitochondrial DNA Sequencing
ComparisonCOX15 Gene Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency type 2 NGS Genetic TestCOX15 test is specific for COX15 gene mutations

Frequently Asked Questions

What is COX15 Gene Cardioencephalomyopathy?
It is a rare genetic disorder caused by mutations in the COX15 gene, leading to cytochrome c oxidase deficiency and severe symptoms in infants.
What are the symptoms of this condition?
Symptoms include developmental delays, seizures, muscle weakness, feeding difficulties, respiratory failure, neurological impairment, and cardiomyopathy.
How is COX15 Gene Cardioencephalomyopathy diagnosed?
Diagnosis is through Next-Generation Sequencing (NGS) genetic testing to identify mutations in the COX15 gene.
What is the cost of the NGS Genetic Test?
The test costs INR 20,000 at DNA Labs India.
Is the test covered by insurance?
Coverage varies; patients should check with their insurance provider.
How long does it take to get the test results?
Results are typically available in 3 to 4 weeks.
What sample is required for the test?
Blood, extracted DNA, or one drop of blood on an FTA card.
Is home sample collection available?
Yes, free home collection is offered for online bookings.
Who should consider this genetic test?
Infants or children with symptoms of mitochondrial disorders or a family history of COX15-related conditions.
What is the treatment for COX15 Gene Cardioencephalomyopathy?
There is no cure; management is supportive and focuses on symptom relief.
How accurate is the NGS Genetic Test?
NGS is highly sensitive and specific for detecting COX15 gene mutations.
Can this test be done at any age?
Yes, the test can be performed at any age, but it is most relevant for infants and young children.
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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