KCNJ1 Gene Bartter Syndrome Type 2 NGS Genetic DNA Test
Introduction to the KCNJ1 Gene Bartter Syndrome Type 2 NGS Genetic DNA Test
The KCNJ1 Gene Bartter Syndrome Type 2 NGS Genetic DNA Test is a specialized diagnostic tool that allows healthcare professionals to identify genetic mutations associated with Bartter syndrome type 2. This condition primarily affects kidney function, leading to imbalances in electrolytes and impacting overall health. Understanding your genetic predisposition through this test is essential for early diagnosis and management of the condition.
What the Test Measures
This genetic test specifically detects mutations in the KCNJ1 gene, which encodes a potassium channel crucial for kidney function. By analyzing the genetic material, healthcare providers can ascertain whether an individual carries mutations that may lead to Bartter syndrome type 2.
Who Should Consider This Test?
Individuals who experience symptoms such as:
- Frequent dehydration
- Muscle weakness
- Growth retardation in children
- Increased urination
are encouraged to consider this test. Additionally, those with a family history of Bartter syndrome or related kidney disorders should also seek testing, as genetic predisposition plays a significant role in the disease.
Benefits of Taking the Test
- Early diagnosis and intervention can prevent complications.
- Informed decisions regarding treatment and management options.
- Understanding family risk and implications for relatives.
- Access to tailored healthcare and genetic counseling.
Understanding Your Results
Results from the KCNJ1 Gene Bartter Syndrome Type 2 NGS Genetic DNA Test will be interpreted by qualified healthcare professionals. A positive result indicates the presence of mutations linked to Bartter syndrome, while a negative result suggests no identified genetic risk. It is essential to discuss your results with a healthcare provider to understand their implications fully.
Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| KCNJ1 Gene Bartter Syndrome Type 2 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To ensure a smooth testing process, please prepare by providing a clinical history and consider a genetic counseling session to discuss family history related to Bartter syndrome. The turnaround time for results is approximately 3 to 4 weeks.
For inquiries and to book your test, please call or WhatsApp us at +2348077798758. Don’t wait to take control of your health!
