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MTTN Gene Mitochondrial Complex I Deficiency Genetic Test

Original price was: $700.Current price is: $500.

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The MTTN Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the MT-TN gene responsible for mitochondrial complex I deficiency. This comprehensive test helps diagnose rare neurological disorders affecting energy production in cells. Using Next-Generation Sequencing (NGS) technology, the test provides precise detection of genetic variants that impair mitochondrial function. Patients experiencing symptoms like muscle weakness, developmental delays, or neurological abnormalities benefit from this diagnostic tool. The test costs $500 USD and includes professional genetic counseling to help interpret results and understand inheritance patterns. Early detection through this test enables better management strategies and family planning decisions.

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MTTN Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test

Comprehensive Introduction to Mitochondrial Complex I Deficiency Testing

The MTTN Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise identification of mutations in the MT-TN gene that cause mitochondrial complex I deficiency. This sophisticated testing methodology provides crucial insights into rare mitochondrial disorders that affect cellular energy production, enabling accurate diagnosis and personalized treatment approaches for patients experiencing complex neurological symptoms.

What This Advanced Genetic Test Measures and Detects

This comprehensive NGS-based genetic test specifically targets and analyzes the MT-TN gene, which encodes a transfer RNA essential for mitochondrial protein synthesis. The test identifies:

  • Pathogenic variants in the MT-TN gene that disrupt mitochondrial complex I function
  • Point mutations, deletions, and insertions affecting mitochondrial energy production
  • Genetic abnormalities that impair oxidative phosphorylation processes
  • Inheritance patterns of mitochondrial DNA mutations
  • Specific genetic markers associated with neurological manifestations

Who Should Consider MTTN Gene Testing

This specialized genetic test is recommended for individuals presenting with symptoms suggestive of mitochondrial disorders, including:

  • Progressive muscle weakness and exercise intolerance
  • Developmental delays in infants and children
  • Neurological abnormalities such as seizures or movement disorders
  • Vision or hearing problems related to mitochondrial dysfunction
  • Family history of mitochondrial disease or unexplained neurological conditions
  • Unexplained metabolic acidosis or lactic acidosis
  • Patients with suspected Leigh syndrome or similar mitochondrial encephalopathies

Significant Benefits of MTTN Genetic Testing

Undergoing the MTTN Gene Mitochondrial Complex I Deficiency test provides numerous advantages:

  • Accurate diagnosis leading to targeted treatment strategies
  • Early intervention opportunities for better disease management
  • Clear understanding of inheritance patterns for family planning
  • Elimination of diagnostic uncertainty and unnecessary testing
  • Access to specialized mitochondrial disease management protocols
  • Improved quality of life through personalized care approaches
  • Potential participation in clinical trials and research studies

Understanding Your Test Results

Our comprehensive genetic counseling services help you interpret your MTTN gene test results effectively:

  • Positive Result: Indicates the presence of pathogenic MT-TN gene mutations, confirming mitochondrial complex I deficiency diagnosis
  • Negative Result: Suggests no detectable mutations in the MT-TN gene, though other mitochondrial genes may require evaluation
  • Variant of Uncertain Significance: Identifies genetic changes with unclear clinical implications, requiring ongoing monitoring
  • Carrier Status: Determines if individuals carry mutations that could be passed to offspring

Our expert genetic counselors provide detailed explanations of your results, discuss implications for family members, and guide you through next steps in management and treatment.

Test Pricing and Details

Test Feature Details
Test Name MTTN Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Specialty Neurologist
Department Genetics
Testing Method NGS Technology
Disease Category Neurological Disorders

Nationwide Testing Availability

We proudly offer the MTTN Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test at our state-of-the-art facilities across the United States. Our branches are conveniently located in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, and many other cities. Each location is equipped with advanced genetic testing technology and staffed by experienced genetic specialists dedicated to providing accurate and compassionate care.

Take Control of Your Neurological Health Today

Don’t let uncertainty about mitochondrial disorders affect your quality of life. Our comprehensive MTTN gene testing provides the clarity you need for proper diagnosis and management. With our discounted price of $500 USD and expert genetic counseling included, you can make informed decisions about your health and future.

Call or WhatsApp us now at +1(267) 388-9828 to schedule your appointment or book your test online. Our genetic specialists are ready to guide you through the testing process and help you understand your results with compassion and expertise.