SCNN1B Gene Liddle Syndrome NGS Genetic DNA Test
Introduction to the Test
The SCNN1B Gene Liddle Syndrome NGS Genetic DNA Test is an advanced diagnostic tool designed to identify mutations in the SCNN1B gene, which are associated with Liddle syndrome. This condition can lead to severe kidney dysfunction and hypertension. Understanding your genetic predisposition is crucial for proactive health management.
What the Test Measures
This test specifically measures genetic variations in the SCNN1B gene using Next Generation Sequencing (NGS) technology. By analyzing your DNA, we can determine if you carry mutations that may predispose you to Liddle syndrome.
Who Should Consider This Test?
Individuals with a family history of Liddle syndrome or symptoms such as hypertension, hypokalemia, and metabolic alkalosis should consider this test. Additionally, those with unexplained kidney issues or endocrine disorders may benefit from understanding their genetic risks.
Benefits of Taking the Test
- Early detection of genetic predisposition to Liddle syndrome.
- Informed decision-making regarding health management and lifestyle adjustments.
- Guidance for family planning and understanding hereditary risks.
- Access to personalized medical care tailored to your genetic profile.
Understanding Your Results
Once the test is completed, our genetic counselors will assist you in interpreting the results. A positive result indicates the presence of mutations associated with Liddle syndrome, while a negative result suggests no identified genetic risk. It is important to discuss these results with your healthcare provider for comprehensive management.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SCNN1B Gene Liddle Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to understand your genetic health. Book the SCNN1B Gene Liddle Syndrome NGS Genetic DNA Test today by calling or WhatsApp messaging us at +2348110567037. Take control of your health and make informed decisions for your future.
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 SCNN1B gene.
This test falls under the specialty of General Physician and the department of Genetics, focusing on Hepatology, Nephrology, and Endocrinology disorders.
