DPYD Gene Dihydropyrimidine Dehydrogenase Deficiency NGS Genetic DNA Test
Introduction
The DPYD Gene Dihydropyrimidine Dehydrogenase Deficiency NGS Genetic DNA Test is a crucial diagnostic tool that helps identify genetic predispositions to metabolic disorders, particularly those affecting the metabolism of certain medications. This test is significant for individuals who may be at risk of experiencing adverse drug reactions due to variations in the DPYD gene, which plays a vital role in drug metabolism.
What the Test Measures
This genetic test specifically measures variations in the DPYD gene, which encodes the enzyme dihydropyrimidine dehydrogenase (DPD). DPD is essential for the metabolism of pyrimidine analogs, commonly used in cancer treatments. Deficiencies in this enzyme can lead to severe toxicity and adverse effects in patients undergoing chemotherapy.
Who Should Consider This Test
Patients who are prescribed medications such as fluorouracil or capecitabine should consider undergoing the DPYD Gene Dihydropyrimidine Dehydrogenase Deficiency NGS Genetic DNA Test. Additionally, those with a family history of DPD deficiency or related metabolic disorders should also seek this test. Symptoms indicating a potential issue with drug metabolism may include severe side effects from medications and unexplained adverse reactions.
Benefits of Taking the Test
- Identifies genetic predisposition to DPD deficiency.
- Helps in personalizing medication plans to avoid adverse reactions.
- Provides peace of mind for patients and their families.
- Facilitates informed decision-making regarding cancer treatment options.
Understanding Your Results
Upon completion of the test, results will be analyzed to determine the presence of any genetic variations in the DPYD gene. A genetic counseling session is recommended to help interpret these results and discuss potential implications for treatment plans.
Test Details
| Test Name | Discount Price | Regular Price |
|---|---|---|
| DPYD Gene Dihydropyrimidine Dehydrogenase Deficiency NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Booking the Test
To book the DPYD Gene Dihydropyrimidine Dehydrogenase Deficiency NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website to schedule your appointment. Ensure you have a clinical history and consider a genetic counseling session to discuss your family’s medical history concerning DPD deficiency.
Test Specifications
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical History of Patient and Genetic Counseling session to draw a pedigree chart of family members affected with Dihydropyrimidine Dehydrogenase Deficiency.
This test is performed under the specialty of General Physician in the Genetics department using NGS Technology, focusing on metabolic disorders.
