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COMT Gene Catechol-O-Methyltransferase Deficiency Genetic Test

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

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The COMT Gene Catechol-O-Methyltransferase Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the COMT gene responsible for regulating neurotransmitters like dopamine and norepinephrine. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect genetic variations that can lead to metabolic disorders affecting mental health, pain perception, and stress response. Individuals experiencing unexplained mood disorders, chronic pain conditions, or cognitive challenges should consider this test. The results provide valuable insights for personalized treatment approaches and genetic counseling. Available for $500 USD, this test offers a detailed analysis of your genetic predisposition to catecholamine-related metabolic conditions.

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COMT Gene Catechol-O-Methyltransferase Deficiency NGS Genetic DNA Test

Understanding COMT Gene Deficiency and Its Clinical Significance

The COMT Gene Catechol-O-Methyltransferase Deficiency NGS Genetic DNA Test represents a breakthrough in personalized medicine, offering comprehensive analysis of genetic variations that impact neurotransmitter metabolism. Catechol-O-methyltransferase (COMT) is a crucial enzyme responsible for breaking down catecholamines, including dopamine, norepinephrine, and epinephrine. These neurotransmitters play vital roles in mood regulation, stress response, pain perception, and cognitive function.

When COMT enzyme activity is compromised due to genetic mutations, individuals may experience altered neurotransmitter levels that can contribute to various health conditions. Our advanced NGS technology provides detailed insights into your genetic makeup, enabling healthcare providers to develop targeted treatment strategies based on your unique genetic profile.

What Does the COMT Gene Test Measure and Detect?

This sophisticated genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the complete COMT gene sequence, identifying:

  • Single nucleotide polymorphisms (SNPs) affecting enzyme activity
  • Missense mutations that alter protein structure
  • Frameshift mutations impacting gene function
  • Copy number variations affecting gene dosage
  • Regulatory region mutations influencing gene expression

The test specifically examines the Val158Met polymorphism, one of the most clinically significant variations in the COMT gene that affects enzyme thermostability and activity levels. This comprehensive analysis provides a complete picture of your genetic predisposition to catecholamine-related metabolic disorders.

Who Should Consider COMT Gene Testing?

Clinical Indications and Symptoms

This genetic test is particularly valuable for individuals experiencing:

  • Unexplained mood disorders or emotional instability
  • Chronic pain conditions unresponsive to conventional treatments
  • Cognitive challenges including memory and attention issues
  • Heightened stress sensitivity and anxiety disorders
  • Family history of neurotransmitter-related conditions
  • Adverse reactions to certain medications metabolized by COMT
  • Metabolic disorders affecting neurotransmitter balance

Benefits of COMT Gene Deficiency Testing

Undergoing COMT gene analysis provides numerous advantages for personalized healthcare:

  • Personalized Treatment Planning: Results guide medication selection and dosing based on your metabolic profile
  • Early Intervention Opportunities: Identify genetic predispositions before symptoms become severe
  • Improved Mental Health Management: Tailor psychiatric treatments to your neurotransmitter metabolism
  • Enhanced Pain Management: Develop targeted pain control strategies based on genetic factors
  • Family Planning Insights: Understand inheritance patterns for genetic counseling
  • Lifestyle Optimization: Implement dietary and exercise regimens that complement your genetic makeup

Understanding Your Test Results

Your COMT gene test results will be carefully interpreted by our genetic specialists and presented in an easy-to-understand format:

Result Interpretation Guidelines

  • Normal Variants: Common polymorphisms with minimal clinical significance
  • Intermediate Activity: Moderate enzyme function alterations requiring monitoring
  • Significant Mutations: Clinically relevant variations impacting neurotransmitter metabolism
  • Pathogenic Variants: Disease-causing mutations requiring medical intervention

All results include detailed explanations and recommendations for next steps. Our genetic counselors are available to help you understand your results and discuss appropriate management strategies with your healthcare provider.

Test Details and Pricing

Test Feature Details
Test Name COMT Gene Catechol-O-Methyltransferase Deficiency NGS Genetic DNA Test
Regular Price $700 USD
Discount Price $500 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next-Generation Sequencing (NGS) Technology

Nationwide Testing Availability

We have conveniently located testing centers across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure accurate sample collection and processing, with genetic counseling services available at all locations.

Take Control of Your Genetic Health Today

Understanding your COMT gene status can provide crucial insights into your neurotransmitter metabolism and overall health. Our comprehensive genetic testing service combines advanced technology with expert interpretation to deliver meaningful results that can guide your healthcare decisions.

Ready to unlock the secrets of your genetic makeup? Contact us today to schedule your COMT Gene Catechol-O-Methyltransferase Deficiency NGS Genetic DNA Test. Call or WhatsApp us at +1(267) 388-9828 to book your appointment or speak with our genetic counseling team.

Take the first step toward personalized healthcare based on your unique genetic profile. Our team is ready to help you understand your results and develop a comprehensive management plan tailored to your specific needs.