TRPC6 Gene Focal Segmental Glomerulosclerosis Type 2 NGS Genetic DNA Test
Introduction
The TRPC6 Gene Focal Segmental Glomerulosclerosis Type 2 NGS Genetic DNA Test is a specialized diagnostic tool designed to detect genetic mutations associated with focal segmental glomerulosclerosis (FSGS), a serious kidney condition. By utilizing Next-Generation Sequencing (NGS) technology, this test provides comprehensive insights into the TRPC6 gene, which plays a crucial role in kidney function.
What the Test Measures
This test specifically measures mutations in the TRPC6 gene, which can lead to FSGS and other nephrological disorders. By identifying these mutations, healthcare providers can better understand the underlying causes of kidney dysfunction in patients.
Who Should Consider This Test?
Individuals who exhibit symptoms such as swelling in the legs and ankles, proteinuria, and high blood pressure may benefit from this test. Additionally, those with a family history of kidney diseases should consider genetic testing to assess their risk factors.
Benefits of Taking the Test
- Early detection of genetic predispositions to kidney disorders.
- Informed decision-making regarding treatment options.
- Guidance for family members who may also be at risk.
- Access to tailored management strategies for kidney health.
Understanding Your Results
Results from the TRPC6 Gene Focal Segmental Glomerulosclerosis Type 2 NGS Genetic DNA Test will indicate whether or not mutations are present in the TRPC6 gene. A positive result may suggest a higher risk for developing kidney disorders, while a negative result may provide reassurance. It’s important to discuss your results with a healthcare professional to understand their implications fully.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| TRPC6 Gene Focal Segmental Glomerulosclerosis Type 2 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking Information
To book the TRPC6 Gene Focal Segmental Glomerulosclerosis Type 2 NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Ensure you have your clinical history and consider a genetic counseling session to discuss your family’s health background.
Test Details
- 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 the patient and a genetic counseling session to draw a pedigree chart of affected family members.
This test is conducted under the specialty of General Physician, within the Genetics department, utilizing NGS technology, and focuses on Hepatology, Nephrology, and Endocrinology disorders.
