COMT Gene Catecholomethyltransferase Deficiency NGS Genetic DNA Test
Introduction
The COMT Gene Catecholomethyltransferase Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic variations associated with catechol-o-methyltransferase (COMT) deficiency. This condition can lead to various metabolic disorders, impacting the body’s ability to metabolize neurotransmitters and hormones effectively. Understanding your genetic makeup through this test can provide valuable insights into your health and potential risks.
What the Test Measures
This genetic test analyzes the COMT gene to detect mutations that may cause deficiencies in the enzyme responsible for breaking down catecholamines, which include dopamine, epinephrine, and norepinephrine. By identifying these genetic variations, healthcare providers can better understand a patient’s metabolic profile.
Who Should Consider This Test
The COMT Gene Catecholomethyltransferase Deficiency NGS Genetic DNA Test is particularly recommended for individuals experiencing:
- Symptoms of mood disorders, anxiety, or depression
- Family history of metabolic disorders
- Unexplained neurological symptoms
- Patients undergoing genetic counseling for inherited conditions
Benefits of Taking the Test
Taking the COMT Gene test offers several benefits, including:
- Early detection of potential metabolic disorders
- Personalized treatment plans based on genetic predisposition
- Informed lifestyle and dietary choices to manage symptoms
- Better understanding of family health history and risks
Understanding Your Results
Results from the COMT Gene test will indicate whether any genetic variations were detected. A genetic counselor will help interpret these results and discuss their implications for your health and family members. It is essential to have a clinical history and possibly a pedigree chart prepared during the genetic counseling session prior to testing.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| COMT Gene Catecholomethyltransferase Deficiency NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Additional Information
Turnaround time for the test results is approximately 3 to 4 weeks. The sample type required can be blood, extracted DNA, or even a single drop of blood on an FTA card. We have branches across all major cities in Kenya, and we also offer home sample collection services for your convenience.
Book Your Test Today!
Don’t wait to learn more about your genetic health. Book the COMT Gene Catecholomethyltransferase Deficiency NGS Genetic DNA Test today by calling or WhatsApping us at +254711564616. Take the first step towards understanding your health better!
