NPHS1 Gene Nephrosis Finnish Type NGS Genetic DNA Test
Introduction
The NPHS1 Gene Nephrosis Finnish Type NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the NPHS1 gene, which are associated with Finnish-type nephrosis. This condition is characterized by kidney dysfunction, leading to proteinuria and potential kidney failure. Early detection through this test is vital for managing the condition effectively and preventing severe complications.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to analyze the NPHS1 gene. It detects specific mutations that may cause nephrosis, providing valuable information about an individual’s genetic predisposition to kidney-related disorders.
Who Should Consider This Test
Individuals with a family history of nephrosis or those experiencing symptoms such as:
- Swelling in the legs or abdomen
- Foamy urine
- Fatigue
- High blood pressure
should consider this test. Additionally, patients with a clinical history suggestive of kidney dysfunction may benefit from this genetic assessment.
Benefits of Taking the Test
- Early diagnosis of potential genetic kidney disorders.
- Informed decision-making regarding treatment and management options.
- Understanding family risk and implications for relatives.
- Access to personalized healthcare strategies based on genetic findings.
Understanding Your Results
Results from the NPHS1 Gene Nephrosis test will indicate whether any mutations were detected in the NPHS1 gene. A genetic counseling session will help interpret these results, providing insights into the implications for your health and potential next steps.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
NPHS1 Gene Nephrosis Finnish Type NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To book the NPHS1 Gene Nephrosis Finnish Type NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our team is ready to assist you with the booking process and any inquiries you may have.
Pre-Test Instructions
Before undergoing the NPHS1 Gene Nephrosis test, it is essential to have a clinical history assessment and a genetic counseling session. This session will help draw a pedigree chart of family members affected by NPHS1 gene nephrosis, ensuring a comprehensive understanding of your genetic background.
Specialty and Department
This test falls under the specialty of General Physician and is conducted in the Genetics department using NGS technology, focusing on hepatology, nephrology, and endocrinology disorders.