TBXAS1 Gene Thromboxane Synthase Deficiency NGS Genetic DNA Test
Introduction
The TBXAS1 Gene Thromboxane Synthase Deficiency NGS Genetic DNA Test is a specialized diagnostic tool that analyzes the TBXAS1 gene for mutations. This test is essential for understanding thromboxane synthase deficiency, a condition that can lead to various hematological disorders. By identifying genetic predispositions, patients can take proactive steps in managing their health.
What the Test Measures
This genetic test detects mutations in the TBXAS1 gene, which is responsible for producing thromboxane synthase, an enzyme crucial for platelet function and vascular health. Any deficiency can result in significant health issues, including bleeding disorders.
Who Should Consider This Test
Individuals with a family history of thromboxane synthase deficiency or related hematological conditions should consider this test. Symptoms that may warrant testing include:
- Unexplained bleeding or bruising
- Frequent nosebleeds
- Heavy menstrual bleeding
- Family history of blood disorders
Benefits of Taking the Test
Taking the TBXAS1 Gene Thromboxane Synthase Deficiency NGS Genetic DNA Test can provide several benefits:
- Early detection of genetic disorders
- Informed decision-making regarding treatment options
- Guidance for family planning and genetic counseling
- Personalized healthcare management
Understanding Your Results
Results from the TBXAS1 test will indicate whether mutations are present in the TBXAS1 gene. A genetic counselor will help interpret these results, providing insights into potential health implications and the next steps in management.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today
To schedule your TBXAS1 Gene Thromboxane Synthase Deficiency NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our team at DNA Labs Nigeria is ready to assist you in understanding your genetic health.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with the TBXAS1 gene are required.
