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NGSMito Comprehensive Genetic Test

Original price was: $750.Current price is: $500.

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The NGSMito Comprehensive NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes next-generation sequencing technology to analyze mitochondrial DNA for comprehensive genetic insights. This advanced test detects mutations and variations in mitochondrial genes that can cause various neurological disorders and metabolic conditions. By examining the complete mitochondrial genome, it provides crucial information about energy production efficiency and cellular function. The test is particularly valuable for individuals experiencing unexplained neurological symptoms, muscle weakness, or metabolic issues. With results available in 3-4 weeks and a discounted price of $500 USD (regularly $750 USD), this test offers accessible advanced genetic analysis. Sample collection is convenient through blood, extracted DNA, or a simple blood drop on an FTA card. Genetic counseling is recommended prior to testing to ensure proper interpretation and family history documentation.

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NGSMito Comprehensive NGS Genetic DNA Test

Advanced Mitochondrial DNA Analysis for Neurological Health

The NGSMito Comprehensive NGS Genetic DNA Test represents a breakthrough in genetic diagnostics, utilizing state-of-the-art next-generation sequencing technology to provide comprehensive analysis of mitochondrial DNA. Mitochondria, often called the “powerhouses” of cells, play a crucial role in energy production and cellular function. When mitochondrial DNA contains mutations, it can lead to various neurological disorders and metabolic conditions that significantly impact quality of life.

What Does the NGSMito Test Measure?

This comprehensive genetic test analyzes the complete mitochondrial genome to identify:

  • Point mutations in mitochondrial DNA
  • Large-scale deletions and rearrangements
  • Heteroplasmy levels (mixture of normal and mutated mitochondrial DNA)
  • Variations affecting oxidative phosphorylation
  • Mutations associated with mitochondrial encephalomyopathy
  • Genetic markers for Leigh syndrome and MELAS

Who Should Consider This Test?

The NGSMito Comprehensive NGS Genetic DNA Test is recommended for individuals experiencing:

  • Unexplained neurological symptoms including seizures or developmental delays
  • Progressive muscle weakness or exercise intolerance
  • Vision or hearing loss of unknown origin
  • Metabolic disorders affecting multiple organ systems
  • Family history of mitochondrial diseases
  • Unexplained fatigue and energy production issues
  • Suspected mitochondrial disorders in children or adults

Key Benefits of NGSMito Testing

Choosing the NGSMito Comprehensive NGS Genetic DNA Test provides numerous advantages:

  • Comprehensive Analysis: Examines the entire mitochondrial genome for complete genetic assessment
  • Early Detection: Identifies mitochondrial disorders before severe symptoms develop
  • Personalized Treatment: Enables targeted therapeutic approaches based on specific mutations
  • Family Planning: Provides crucial information for genetic counseling and family planning decisions
  • Accurate Diagnosis: Reduces diagnostic uncertainty and unnecessary medical procedures
  • Advanced Technology: Utilizes cutting-edge NGS methodology for superior accuracy

Understanding Your Test Results

Your NGSMito Comprehensive NGS Genetic DNA Test results will be carefully interpreted by our genetic specialists:

  • Normal Results: No significant mitochondrial DNA mutations detected
  • Pathogenic Variants: Identified mutations known to cause mitochondrial disorders
  • Variants of Uncertain Significance: Genetic changes requiring further investigation
  • Heteroplasmy Levels: Percentage of mutated mitochondrial DNA, indicating disease severity
  • Clinical Correlation: Results interpreted in context of your symptoms and family history

All positive results include detailed explanations and recommendations for follow-up care with neurologists and genetic counselors.

Test Pricing and Details

Test Component Details
Test Name NGSMito Comprehensive NGS Genetic DNA Test
Regular Price $750 USD
Discount Price $500 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Methodology Next-Generation Sequencing (NGS) Technology

Pre-Test Preparation

To ensure optimal testing conditions and accurate results:

  • Provide complete clinical history including neurological symptoms
  • Participate in genetic counseling session before testing
  • Prepare detailed family medical history with pedigree chart
  • Document affected family members and their specific conditions
  • Discuss testing implications with your healthcare provider

Nationwide Availability

We have diagnostic centers conveniently located across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, Austin, Jacksonville, Fort Worth, Columbus, Charlotte, San Francisco, Indianapolis, Seattle, Denver, Washington DC, Boston, El Paso, Nashville, Detroit, Oklahoma City, Portland, Las Vegas, Memphis, Louisville, Baltimore, and Milwaukee. Our network ensures accessible genetic testing services nationwide.

Take Control of Your Neurological Health

Don’t let unexplained symptoms compromise your quality of life. The NGSMito Comprehensive NGS Genetic DNA Test provides the answers you need for proper diagnosis and targeted treatment. Our team of genetic specialists and neurologists are ready to help you understand your genetic profile and develop an appropriate management plan.

Ready to uncover the genetic factors affecting your neurological health? Book your NGSMito Comprehensive NGS Genetic DNA Test today by calling our genetic counseling team at +1(267) 388-9828 or schedule your appointment online. Take the first step toward personalized neurological care and genetic clarity.