CLCNKB Gene Bartter Syndrome Type 3 NGS Genetic DNA Test
Introduction
The CLCNKB Gene Bartter Syndrome Type 3 NGS Genetic DNA Test is a specialized genetic examination designed to identify mutations in the CLCNKB gene, which are linked to Bartter syndrome. This condition is a rare genetic disorder that affects kidney function, leading to imbalances in electrolytes and fluid. Understanding the genetic basis of this syndrome is crucial for effective management and treatment options.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to detect specific mutations in the CLCNKB gene. By analyzing the DNA sample, the test can confirm the presence of genetic variations that contribute to Bartter syndrome, facilitating accurate diagnosis and personalized treatment plans.
Who Should Consider This Test
Individuals exhibiting symptoms of Bartter syndrome, such as:
- Excessive thirst and urination
- Low blood pressure
- Muscle weakness or cramps
- Growth issues in children
Additionally, those with a family history of kidney disorders or Bartter syndrome should consider this test as part of their diagnostic process.
Benefits of Taking the Test
- Accurate identification of genetic mutations associated with Bartter syndrome.
- Guides treatment decisions and management strategies for affected individuals.
- Provides valuable information for family planning and genetic counseling.
- Enhances understanding of the disease’s hereditary nature.
Understanding Your Results
Results from the CLCNKB Gene Bartter Syndrome Type 3 NGS Genetic DNA Test will indicate whether mutations are present in the CLCNKB gene. A positive result confirms the diagnosis of Bartter syndrome, while a negative result may suggest other underlying issues or conditions. It is essential to discuss your results with a healthcare professional for comprehensive interpretation and advice.
Pricing Information
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book your CLCNKB Gene Bartter Syndrome Type 3 NGS Genetic DNA Test, contact us at +2348077798758. Our team is ready to assist you with the booking process and answer any questions you may have.
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 going for the test is required. A genetic counseling session to draw a pedigree chart of family members affected by Bartter syndrome is also recommended.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Hepatology, Nephrology, Endocrinology Disorders
