COX15 Gene Leigh Syndrome NGS Genetic DNA Test
Comprehensive Genetic Testing for Mitochondrial Disorders
The COX15 Gene Leigh Syndrome NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise detection of mutations associated with Leigh syndrome. This sophisticated test utilizes advanced Next-Generation Sequencing technology to analyze the COX15 gene, which plays a critical role in mitochondrial energy production and cellular function.
What This Test Measures and Detects
This comprehensive genetic analysis specifically targets:
- Mutations in the COX15 gene that impair cytochrome c oxidase assembly
- Genetic variants affecting mitochondrial complex IV function
- Pathogenic changes leading to impaired cellular energy production
- Inheritance patterns of Leigh syndrome within families
- Specific genetic markers associated with neurological deterioration
Who Should Consider This Genetic Test
This test is particularly recommended for individuals experiencing:
- Progressive neurological deterioration in infancy or childhood
- Developmental regression following periods of normal development
- Muscle weakness, hypotonia, or movement disorders
- Vision problems, including optic atrophy or nystagmus
- Breathing difficulties or respiratory chain dysfunction
- Family history of mitochondrial disorders or Leigh syndrome
- Unexplained metabolic acidosis or elevated lactate levels
Significant Benefits of COX15 Genetic Testing
Undergoing this advanced genetic analysis provides numerous advantages:
- Accurate Diagnosis: Precise identification of COX15 gene mutations enables definitive diagnosis
- Personalized Treatment: Results guide targeted therapeutic interventions and management strategies
- Family Planning: Essential information for genetic counseling and reproductive decision-making
- Proactive Management: Early detection allows for timely intervention and symptom management
- Research Contribution: Participation advances understanding of mitochondrial disorders
Understanding Your Test Results
Our comprehensive genetic counseling ensures you fully comprehend your results:
- Positive Result: Indicates presence of pathogenic COX15 mutations, confirming Leigh syndrome diagnosis
- Negative Result: Suggests absence of detectable COX15 mutations, though other genetic causes may exist
- Variant of Uncertain Significance: Requires additional family studies and clinical correlation
- Carrier Status: Identifies individuals who may pass mutations to offspring without showing symptoms
Test Pricing and Details
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type | Blood, Extracted DNA, or One Drop Blood on FTA Card |
Pre-Test Requirements
Before testing, we require:
- Complete clinical history of the patient
- Genetic counseling session to create detailed family pedigree
- Documentation of affected family members with neurological symptoms
- Review of previous neurological evaluations and test results
Nationwide Accessibility
We proudly serve patients across the United States with convenient testing locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified genetic counselors and neurological specialists ensures comprehensive care regardless of your location.
Take Control of Your Genetic Health Today
Don’t let uncertainty about neurological symptoms affect your quality of life. Our COX15 Gene Leigh Syndrome NGS Genetic DNA Test provides the clarity needed for informed medical decisions and personalized care planning. With our discounted price of $500 USD and comprehensive genetic counseling services, you can access world-class neurological genetic testing.
Call or WhatsApp us now at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our expert team is ready to guide you through every step of the testing process and help you understand your results with compassion and expertise.
