SLC12A3 Gene Bartter Syndrome NGS Genetic DNA Test
Introduction to the Test
The SLC12A3 Gene Bartter Syndrome NGS Genetic DNA Test is a state-of-the-art diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to analyze the SLC12A3 gene. This test is essential for diagnosing Bartter syndrome, a rare genetic disorder that affects kidney function and electrolyte balance. Understanding your genetic predisposition can lead to better management and treatment options.
What the Test Measures
This genetic test specifically measures mutations in the SLC12A3 gene, which plays a crucial role in kidney function. By identifying these mutations, healthcare providers can assess the risk of developing Bartter syndrome and related complications.
Who Should Consider This Test?
Individuals who should consider the SLC12A3 Gene Bartter Syndrome NGS Genetic DNA Test include:
- Those experiencing symptoms such as excessive thirst, frequent urination, muscle weakness, or fatigue.
- Individuals with a family history of Bartter syndrome or related kidney disorders.
- Patients with unexplained electrolyte imbalances.
Benefits of Taking the Test
Taking the SLC12A3 Gene Bartter Syndrome NGS Genetic DNA Test offers numerous benefits, including:
- Early diagnosis and intervention for Bartter syndrome.
- Informed decision-making regarding treatment options.
- Better management of symptoms and prevention of complications.
- Genetic counseling for affected family members.
Understanding Your Results
After the test, results will indicate whether mutations in the SLC12A3 gene are present. It is important to discuss these results with a healthcare provider to understand their implications fully. General guidance will be provided to help manage any identified risks.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| SLC12A3 Gene Bartter Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the SLC12A3 Gene Bartter Syndrome NGS Genetic DNA Test, please contact us at +2348077798758 via call or WhatsApp. Our team is ready to assist you in scheduling your appointment and addressing any questions you may have.
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 Patient and a Genetic Counseling session to draw a pedigree chart of family members affected with SLC12A3 Gene Bartter syndrome.
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Hepatology, Nephrology, Endocrinology Disorders
