NR3C2 Gene Pseudohypoaldosteronism Type 1 Autosomal Dominant NGS Genetic DNA Test
The NR3C2 Gene Pseudohypoaldosteronism Type 1 Autosomal Dominant NGS Genetic DNA Test is a pivotal diagnostic tool that helps identify genetic mutations associated with pseudohypoaldosteronism, a condition that affects the body’s ability to regulate sodium and potassium levels. Understanding this genetic predisposition is crucial for managing related health issues effectively.
What the Test Measures
This test specifically detects mutations in the NR3C2 gene, which encodes the mineralocorticoid receptor. This receptor plays a vital role in regulating electrolyte balance, blood pressure, and overall fluid homeostasis.
Who Should Consider This Test
- Individuals with symptoms of pseudohypoaldosteronism, such as high levels of potassium or low sodium levels.
- Patients with a family history of endocrine disorders or unexplained hypertension.
- Individuals undergoing genetic counseling for hereditary conditions.
Benefits of Taking the Test
- Early diagnosis can lead to timely management of hormonal imbalances.
- Helps in understanding familial risks and guiding treatment options.
- Provides valuable information for personalized healthcare strategies.
Understanding Your Results
Results from the NR3C2 Gene Pseudohypoaldosteronism test will be interpreted by our qualified genetic counselors. They will provide insights into the implications of your results and recommend further actions or treatments if necessary.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| NR3C2 Gene Pseudohypoaldosteronism Type 1 Autosomal Dominant NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Book Your Test Today!
To schedule your NR3C2 Gene Pseudohypoaldosteronism Type 1 Autosomal Dominant NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with your booking and any questions you may have.
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 who is going for the NR3C2 Gene Pseudohypoaldosteronism Type 1 Autosomal Dominant NGS Genetic DNA Test and a genetic counseling session to draw a pedigree chart of family members affected with the NR3C2 gene.
Our laboratory specializes in Genetics, utilizing NGS Technology to provide accurate and reliable results for conditions related to Hepatology, Nephrology, and Endocrinology disorders.
