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VDAC1 Gene Encephalopathy Mitochondrial Genetic Test

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

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The VDAC1 Gene Encephalopathy Mitochondrial NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the VDAC1 gene, which plays a crucial role in mitochondrial function and neurological health. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect genetic variations associated with mitochondrial encephalopathy, a serious neurological condition affecting brain function and energy metabolism. The test is particularly valuable for individuals experiencing unexplained neurological symptoms, developmental delays, or family history of mitochondrial disorders. Results provide critical information for accurate diagnosis, personalized treatment strategies, and genetic counseling. Available for only $500 USD, this test offers significant insights into mitochondrial health and neurological function, helping patients and healthcare providers make informed decisions about care and management.

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VDAC1 Gene Encephalopathy Mitochondrial NGS Genetic DNA Test

Comprehensive Genetic Testing for Mitochondrial Neurological Disorders

The VDAC1 Gene Encephalopathy Mitochondrial NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise identification of mutations in the VDAC1 (Voltage-Dependent Anion Channel 1) gene. This gene encodes a critical protein located in the mitochondrial outer membrane, playing an essential role in regulating mitochondrial function, energy production, and cellular metabolism. When mutations occur in the VDAC1 gene, they can disrupt mitochondrial integrity and lead to severe neurological conditions known as mitochondrial encephalopathies.

What This Advanced Test Measures

Our comprehensive NGS-based test specifically targets and analyzes the VDAC1 gene to detect:

  • Point mutations and single nucleotide variants affecting mitochondrial function
  • Insertions and deletions that may disrupt protein structure
  • Copy number variations impacting gene dosage
  • Pathogenic variants associated with mitochondrial encephalopathy
  • Genetic markers linked to impaired energy metabolism in brain cells

Who Should Consider This Genetic Test?

This specialized genetic analysis is particularly recommended for individuals experiencing:

  • Unexplained neurological symptoms including seizures, ataxia, or movement disorders
  • Progressive cognitive decline or developmental regression
  • Family history of mitochondrial disorders or unexplained neurological conditions
  • Muscle weakness, exercise intolerance, or fatigue without clear cause
  • Vision or hearing problems potentially related to mitochondrial dysfunction
  • Metabolic abnormalities suggesting mitochondrial disease
  • Children with developmental delays and suspected genetic neurological conditions

Significant Benefits of VDAC1 Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Accurate Diagnosis: Provides definitive identification of VDAC1-related mitochondrial encephalopathy
  • Personalized Treatment: Enables targeted therapeutic approaches based on specific genetic findings
  • Family Planning Guidance: Offers crucial information for genetic counseling and reproductive decisions
  • Prognostic Insights: Helps predict disease progression and potential complications
  • Early Intervention: Facilitates timely management strategies to optimize neurological outcomes
  • Research Contribution: Advances scientific understanding of mitochondrial neurological disorders

Understanding Your Test Results

Our comprehensive report provides detailed interpretation of your genetic findings:

  • Positive Result: Indicates the presence of pathogenic VDAC1 mutations, confirming mitochondrial encephalopathy diagnosis
  • Negative Result: Suggests absence of known VDAC1 mutations, though other genetic causes may need investigation
  • Variant of Uncertain Significance: Identifies genetic changes requiring further clinical correlation
  • Carrier Status: Determines if you carry mutations that could affect future generations

All results are accompanied by detailed explanations and recommendations for next steps, including consultation with our specialized neurologists and genetic counselors.

Test Pricing and Availability

Test Feature Details
Test Name VDAC1 Gene Encephalopathy Mitochondrial 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

Nationwide Accessibility and Convenience

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 collection centers ensures easy access to this advanced genetic testing regardless of your location.

Pre-Test Preparation Requirements

To ensure optimal testing accuracy, we require:

  • Complete clinical history of the patient undergoing testing
  • Genetic counseling session to create detailed family pedigree chart
  • Documentation of affected family members with similar neurological symptoms
  • Comprehensive neurological evaluation findings

Take Control of Your Neurological Health Today

Don’t let unexplained neurological symptoms remain a mystery. Our VDAC1 Gene Encephalopathy Mitochondrial NGS Genetic DNA Test provides the clarity and answers you need for proper diagnosis and targeted treatment. With our discounted price of only $500 USD and comprehensive nationwide coverage, advanced genetic testing has never been more accessible.

Call or WhatsApp us now at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our specialized team is ready to guide you through every step of the testing process and help you understand your results for better neurological health management.