Whole Exome Mitochondrial Genome Sequencing
Comprehensive Mitochondrial DNA Analysis for Advanced Genetic Diagnosis
Whole Exome Mitochondrial Genome Sequencing represents the pinnacle of genetic testing technology, offering unprecedented insights into mitochondrial health and function. Mitochondria, often called the “powerhouses” of our cells, play a critical role in energy production and cellular metabolism. When mitochondrial DNA contains mutations, it can lead to a wide range of debilitating conditions affecting multiple organ systems.
What This Advanced Genetic Test Measures
Our Whole Exome Mitochondrial Genome Sequencing test provides comprehensive analysis of all 37 mitochondrial genes using cutting-edge Next-Generation Sequencing (NGS) technology. This sophisticated testing approach examines:
- Complete mitochondrial DNA sequence analysis
- All 13 protein-coding genes essential for energy production
- 22 transfer RNA genes and 2 ribosomal RNA genes
- Point mutations, deletions, and duplications in mitochondrial DNA
- Heteroplasmy levels (mixture of normal and mutated mitochondrial DNA)
- Maternal inheritance patterns and mutation load
Who Should Consider Mitochondrial Genome Sequencing
This comprehensive genetic test is particularly valuable for individuals experiencing:
- Unexplained neurological symptoms including seizures, developmental delays, or movement disorders
- Progressive muscle weakness, exercise intolerance, or chronic fatigue
- Metabolic disorders with lactic acidosis or abnormal energy metabolism
- Vision or hearing loss of unknown origin
- Multiple organ system involvement without clear diagnosis
- Family history of mitochondrial disorders or unexplained infant deaths
- Children with developmental regression or failure to thrive
- Adults with progressive neurological decline
Significant Benefits of Mitochondrial DNA Testing
Choosing Whole Exome Mitochondrial Genome Sequencing provides numerous advantages for patients and healthcare providers:
- Definitive Diagnosis: Obtain clear answers for complex medical cases that have remained undiagnosed
- Personalized Treatment: Guide therapeutic decisions based on specific mitochondrial mutations
- Family Planning: Understand inheritance patterns and recurrence risks for future pregnancies
- Proactive Management: Implement targeted interventions to manage symptoms and slow disease progression
- Comprehensive Analysis: Single test covering the entire mitochondrial genome instead of multiple targeted tests
- Expert Interpretation: Results reviewed by board-certified geneticists with mitochondrial specialization
Understanding Your Test Results
Our comprehensive report provides detailed interpretation of your mitochondrial genome sequencing results:
- Pathogenic Variants: Clear identification of disease-causing mutations with clinical significance
- Variant Classification: Expert categorization of variants as pathogenic, likely pathogenic, or variants of uncertain significance
- Heteroplasmy Levels: Measurement of mutation load and correlation with disease severity
- Clinical Correlation: Detailed explanation of how identified mutations relate to specific symptoms
- Management Recommendations: Evidence-based guidance for treatment, monitoring, and lifestyle modifications
- Genetic Counseling: Access to genetic counseling services to help understand results and implications
Test Pricing and Availability
| Test Component | Price (USD) |
|---|---|
| Discount Price | $1100 |
| Regular Price | $1750 |
Turnaround Time: 3 to 4 weeks from sample receipt
Sample Type: Blood
Pre-test Requirements: Clinical details are required for comprehensive analysis
Nationwide Testing Availability
We have diagnostic centers conveniently located across the United States, serving patients in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified collection facilities ensures accessible testing regardless of your location.
Take Control of Your Genetic Health Today
Don’t let unexplained symptoms or family history of mitochondrial disorders remain a mystery. Our Whole Exome Mitochondrial Genome Sequencing provides the comprehensive answers you need for accurate diagnosis and effective management. With our discounted price of $1100 USD, advanced genetic testing is more accessible than ever.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or speak with our genetic counseling team. Our expert staff is ready to answer your questions, explain the testing process, and help you take the next step toward understanding your genetic health.
Early diagnosis through comprehensive mitochondrial genome analysis can significantly impact treatment outcomes and quality of life. Book your test now and gain the clarity you deserve for better health management.
