EPHX2 Gene Hypercholesterolemia Familial Due to LDLR Defect Modifier of NGS Genetic DNA Test
Introduction to EPHX2 Gene Testing
The EPHX2 Gene Hypercholesterolemia Familial Due to LDLR Defect Modifier of NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to detect genetic mutations associated with familial hypercholesterolemia (FH), a condition that significantly increases the risk of cardiovascular diseases. This test utilizes Next-Generation Sequencing (NGS) technology to provide a comprehensive analysis of the EPHX2 gene, which plays a crucial role in lipid metabolism.
What the Test Measures
This genetic test specifically measures mutations in the EPHX2 gene that may modify the effects of LDLR defects, which are responsible for the familial form of hypercholesterolemia. By identifying these mutations, healthcare providers can better understand an individual’s risk for developing high cholesterol levels and related complications.
Who Should Consider This Test?
The EPHX2 Gene Hypercholesterolemia test is recommended for individuals who:
- Have a family history of hypercholesterolemia or cardiovascular diseases.
- Exhibit symptoms of high cholesterol such as xanthomas or corneal arcus.
- Are seeking to understand their genetic risk factors for metabolic disorders.
Benefits of Taking the Test
Understanding your genetic predisposition through this test offers several benefits:
- Early identification of individuals at risk for familial hypercholesterolemia.
- Informed decision-making regarding lifestyle changes and treatment options.
- Potential for family screening and genetic counseling, enhancing preventive healthcare.
Understanding Your Results
Results from the EPHX2 Gene Hypercholesterolemia test will indicate whether you carry mutations associated with increased cholesterol levels. It is essential to discuss these results with a healthcare provider who can guide you on the next steps, including lifestyle modifications or treatment options.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400000 |
| Regular Price | 560000 |
Book Your Test Today
Take control of your health by understanding your genetic risks. To book the EPHX2 Gene Hypercholesterolemia Familial Due to LDLR Defect Modifier of NGS Genetic DNA Test, contact us at +2348077798758. Our dedicated team is here to assist you through the process and ensure you receive the best care possible.
Turnaround time for results is approximately 3 to 4 weeks. Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card. Prior to the test, a clinical history and genetic counseling session are recommended to draw a pedigree chart of family members affected with hypercholesterolemia.
