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MT-CO3 Gene Cytochrome C Oxidase 3 Deficiency Genetic Test

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

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The MT-CO3 Gene Cytochrome C Oxidase 3 Deficiency NGS Genetic DNA Test is a comprehensive diagnostic tool that identifies mutations in the MT-CO3 gene responsible for mitochondrial complex IV deficiency. This specialized genetic test utilizes next-generation sequencing technology to detect pathogenic variants that disrupt cellular energy production, leading to severe neurological disorders. The test is essential for individuals experiencing unexplained muscle weakness, developmental delays, exercise intolerance, or family history of mitochondrial diseases. At only $500 USD, this advanced genetic analysis provides crucial information for accurate diagnosis, treatment planning, and genetic counseling. Early detection enables proactive management of mitochondrial disorders and informed family planning decisions.

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MT-CO3 Gene Cytochrome C Oxidase 3 Deficiency NGS Genetic DNA Test

Comprehensive Genetic Testing for Mitochondrial Disorders

The MT-CO3 Gene Cytochrome C Oxidase 3 Deficiency NGS Genetic DNA Test represents a breakthrough in mitochondrial disease diagnosis, offering precise detection of genetic mutations that affect cellular energy production. This advanced genetic analysis targets the MT-CO3 gene, which encodes a critical subunit of cytochrome c oxidase – the final enzyme in the mitochondrial electron transport chain responsible for cellular respiration and ATP generation.

What This Test Measures and Detects

Our specialized NGS genetic test specifically examines the mitochondrial DNA-encoded MT-CO3 gene for pathogenic variants that disrupt cytochrome c oxidase function. The test identifies:

  • Point mutations and small insertions/deletions in the MT-CO3 gene
  • Pathogenic variants affecting complex IV assembly and function
  • Genetic markers associated with mitochondrial encephalomyopathy
  • Inheritance patterns of mitochondrial DNA mutations
  • Risk assessment for developing cytochrome c oxidase deficiency

Who Should Consider This Genetic Test

This comprehensive genetic analysis is recommended for individuals presenting with:

  • Unexplained muscle weakness and exercise intolerance
  • Developmental delays in infants and children
  • Neurological symptoms including seizures and ataxia
  • Family history of mitochondrial disorders
  • Progressive external ophthalmoplegia
  • Cardiomyopathy or cardiac conduction defects
  • Metabolic acidosis and lactic acidosis
  • Failure to thrive in pediatric patients

Clinical Benefits of MT-CO3 Genetic Testing

Undergoing this specialized genetic test provides numerous clinical advantages:

  • Accurate Diagnosis: Confirms or rules out MT-CO3 gene-related disorders
  • Personalized Treatment: Enables targeted therapeutic interventions
  • Family Planning: Provides crucial information for reproductive decisions
  • Prognostic Information: Helps predict disease progression and severity
  • Early Intervention: Facilitates timely management of symptoms
  • Genetic Counseling: Supports informed family risk assessment

Understanding Your Test Results

Our comprehensive genetic report provides detailed interpretation of your MT-CO3 gene analysis:

  • Positive Result: Indicates the presence of pathogenic MT-CO3 variants requiring specialized neurological care and mitochondrial support
  • Negative Result: Suggests typical MT-CO3 gene sequence, though additional testing may be recommended for complex cases
  • Variant of Uncertain Significance: Identifies genetic changes requiring further clinical correlation and family studies
  • Heteroplasmy Levels: Measures the percentage of mutated mitochondrial DNA, crucial for predicting disease severity

Test Pricing and Sample Requirements

Test Component Price (USD)
Discount Price $500
Regular Price $700
Turnaround Time 3-4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card

Pre-Test Requirements

Before undergoing the MT-CO3 Gene Deficiency NGS Test, patients should provide:

  • Complete clinical history documenting neurological symptoms
  • Participation in genetic counseling session
  • Detailed pedigree chart of family members affected by mitochondrial disorders
  • Informed consent for genetic testing and result interpretation

Nationwide Testing Availability

We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more cities nationwide. Our network of certified genetic counselors and neurological specialists ensures comprehensive care throughout your testing journey.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about mitochondrial disorders affect your health decisions. Our MT-CO3 Gene Cytochrome C Oxidase 3 Deficiency NGS Genetic DNA Test provides the definitive answers you need for proper diagnosis and management. With our discounted price of only $500 USD, advanced genetic testing is more accessible than ever.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our experienced genetic specialists are ready to guide you through the testing process and help you understand your results.