Mitochondrial Mutation Detection Comprehensive Panel
Understanding Mitochondrial DNA Testing
Mitochondrial DNA testing represents a cutting-edge approach to diagnosing inherited disorders that affect cellular energy production. Mitochondria, often called the “powerhouses” of our cells, contain their own unique DNA separate from nuclear DNA. When mutations occur in mitochondrial DNA, they can disrupt cellular energy production, leading to a wide range of medical conditions affecting multiple organ systems.
What This Test Measures and Detects
The Mitochondrial Mutation Detection Comprehensive Panel provides comprehensive analysis of key mitochondrial genes essential for cellular energy production:
- ND1, ND4, ND5, ND6 genes: Critical components of complex I in the electron transport chain
- TL1 gene: Involved in mitochondrial protein synthesis
- MCTYB1 gene: Essential for cytochrome b function in complex III
- ATP6 and ATP8 genes: Key subunits of ATP synthase (complex V)
This panel utilizes advanced PCR and sequencing technologies to identify point mutations, deletions, and other genetic variations that can cause mitochondrial dysfunction.
Who Should Consider This Test
This comprehensive mitochondrial testing is recommended for individuals experiencing:
- Unexplained neurological symptoms including seizures, ataxia, or movement disorders
- Progressive muscle weakness or exercise intolerance
- Developmental delays in children
- Metabolic disorders with lactic acidosis
- Vision or hearing loss of unknown cause
- Family history of mitochondrial disorders
- Multiple organ system involvement without clear diagnosis
Benefits of Mitochondrial DNA Testing
- Accurate Diagnosis: Provides definitive diagnosis for complex mitochondrial disorders
- Family Planning: Helps assess inheritance risk for future generations
- Treatment Guidance: Informs targeted treatment approaches and management strategies
- Prognostic Information: Helps predict disease progression and potential complications
- Comprehensive Analysis: Screens multiple mitochondrial genes in a single test
Understanding Your Test Results
Your mitochondrial DNA test results will be carefully interpreted by our expert geneticists and molecular diagnosticians. Results may indicate:
- Pathogenic Mutations: Confirmed disease-causing variants requiring medical management
- Variants of Uncertain Significance: Genetic changes requiring further investigation
- Normal Results: No mitochondrial DNA mutations detected in the tested regions
Our genetic counseling team will provide comprehensive explanations of your results and their implications for your health and family members.
Test Pricing and Details
| Test Component | Price (USD) |
|---|---|
| Discount Price | $750 |
| Regular Price | $1,126 |
| Turnaround Time | Sample Monday by 9 AM; Report Friday |
| Sample Type | 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube |
Convenient Testing Locations Across USA
We have diagnostic centers conveniently located throughout the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure accurate testing and rapid result delivery.
Take Control of Your Genetic Health Today
Don’t let unexplained symptoms continue without answers. Our Mitochondrial Mutation Detection Comprehensive Panel provides the comprehensive genetic analysis needed to understand complex neurological and metabolic conditions. With our discounted price of $750 USD and rapid turnaround time, you can get the answers you need quickly and affordably.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your mitochondrial DNA test and take the first step toward understanding your genetic health.
