SCNN1G Gene Liddle Syndrome NGS Genetic DNA Test
Introduction to the Test
The SCNN1G Gene Liddle Syndrome NGS Genetic DNA Test is designed to identify mutations in the SCNN1G gene, which plays a critical role in renal and electrolyte balance. This test is essential for patients experiencing symptoms related to Liddle syndrome, a condition that can lead to hypertension and other serious health issues.
What the Test Measures
This genetic test utilizes Next-Generation Sequencing (NGS) technology to detect specific mutations in the SCNN1G gene. By analyzing the genetic material, healthcare professionals can determine if a patient has a predisposition to Liddle syndrome and associated disorders.
Who Should Consider This Test?
Patients who exhibit symptoms such as high blood pressure, unexplained electrolyte imbalances, or a family history of Liddle syndrome should consider this test. Risk factors include a personal or family history of hypertension and related kidney disorders.
Benefits of Taking the Test
- Early detection of genetic predisposition to hypertension and related disorders.
- Informed decision-making regarding lifestyle and treatment options.
- Ability to assess risk for family members.
- Access to genetic counseling for better understanding and management.
Understanding Your Results
Results from the SCNN1G Gene Liddle Syndrome NGS Genetic DNA Test typically take 3 to 4 weeks. A genetic counselor will help interpret the results, guiding you through the implications for your health and any necessary follow-up actions.
Test Name and Price
| Discount Price | Regular Price |
|---|---|
| 40000 KSh | 56000 KSh |
Book Your Test Today
We have branches across major cities in Kenya, making it convenient for you to access our services. To book the SCNN1G Gene Liddle Syndrome NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
