TPMT Gene TPMT Deficiency NGS Genetic DNA Test
Introduction
The TPMT Gene TPMT Deficiency NGS Genetic DNA Test is a vital diagnostic tool that assesses the metabolism of thiopurine drugs, which are commonly used in the treatment of various autoimmune disorders and certain cancers. Understanding a patient’s TPMT status can significantly influence treatment decisions, ensuring effective and safe medication management.
What the Test Measures
This test specifically measures the activity of the thiopurine S-methyltransferase (TPMT) enzyme, which is crucial for the metabolism of thiopurine medications. A deficiency in this enzyme can lead to severe toxicity from standard doses of these drugs, making this test essential for patient safety.
Who Should Consider This Test?
Patients who are prescribed thiopurine medications, such as azathioprine or mercaptopurine, should consider this test. It is particularly recommended for individuals with:
- A family history of TPMT deficiency
- Autoimmune diseases requiring thiopurine therapy
- Previous adverse reactions to thiopurine medications
Benefits of Taking the Test
- Identifies patients at risk of drug toxicity, allowing for personalized medication plans.
- Reduces the likelihood of severe side effects associated with thiopurine therapy.
- Informs healthcare providers on the appropriate dosing of thiopurine medications.
Understanding Your Results
Results from the TPMT Gene TPMT Deficiency NGS Genetic DNA Test will indicate whether you have normal, intermediate, or deficient TPMT enzyme activity. Your healthcare provider will guide you on the implications of your results and the best course of action for your treatment plan.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| TPMT Gene TPMT Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the TPMT Gene TPMT Deficiency NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Ensure you have a clinical history ready and consider scheduling a genetic counseling session to discuss any family history related to TPMT deficiency. Your health is our priority, and we are here to assist you every step of the way.
Additional Information
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Department: Genetics
- Method: NGS Technology
- Disease Type: Metabolic Disorders
