COMT Gene Catecholomethyltransferase Deficiency NGS Genetic DNA Test
Introduction to the Test
The COMT Gene Catecholomethyltransferase Deficiency NGS Genetic DNA Test is an advanced diagnostic tool that helps identify genetic variations associated with the catecholamine metabolism process. This test is crucial for individuals who may be at risk of metabolic disorders, allowing for early intervention and tailored treatment plans.
What the Test Measures
This genetic test specifically measures variations in the COMT gene, which plays a significant role in the breakdown of catecholamines—hormones that are vital for regulating mood, stress response, and cognitive function. By analyzing the gene’s functionality, the test can reveal potential deficiencies that may lead to various health issues.
Who Should Consider This Test?
Individuals experiencing symptoms related to mood disorders, anxiety, or cognitive impairments should consider this test. Additionally, those with a family history of metabolic disorders or who have risk factors such as chronic stress or hormonal imbalances may benefit from understanding their genetic predisposition.
Benefits of Taking the Test
- Identifies genetic predispositions to metabolic disorders.
- Informs personalized treatment and management plans.
- Provides insights into mental health and cognitive function.
- Enables early intervention to mitigate potential health issues.
Understanding Your Results
Results from the COMT Gene Catecholomethyltransferase Deficiency NGS Genetic DNA Test will indicate whether genetic variations are present. A genetic counselor will help interpret these results and provide guidance on possible next steps, including lifestyle changes or further testing.
Test Name and Price
| Discount Price | Regular Price |
|---|---|
| 400,000 NGN | 560,000 NGN |
Booking the Test
To book the COMT Gene Catecholomethyltransferase Deficiency NGS Genetic DNA Test, please contact us at +2348110567037. Our team is ready to assist you in scheduling your appointment and answering any questions you may have.
Pre-Test Instructions
Before undergoing the test, it is essential to provide a detailed clinical history and attend a genetic counseling session. This session will help draw a pedigree chart of family members affected by catechol-o-methyltransferase deficiency, ensuring accurate interpretation of your results.
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Metabolic Disorders
