KCNJ5 Gene Hyperaldosteronism Type 3 NGS Genetic DNA Test
Comprehensive Genetic Testing for Hereditary Endocrine Disorders
The KCNJ5 Gene Hyperaldosteronism Type 3 NGS Genetic DNA Test represents a breakthrough in molecular diagnostics for endocrine disorders. This advanced genetic screening utilizes Next-Generation Sequencing technology to detect mutations in the KCNJ5 gene, which plays a critical role in potassium channel function within adrenal gland cells. Understanding your genetic predisposition to hyperaldosteronism type 3 can significantly impact your treatment approach and long-term health outcomes.
What Does This Test Measure?
This sophisticated genetic analysis specifically targets the KCNJ5 gene, which encodes the G protein-activated inward rectifier potassium channel 4. The test identifies:
- Pathogenic variants in the KCNJ5 gene associated with familial hyperaldosteronism type 3
- Specific mutations that cause abnormal aldosterone production
- Genetic markers for inherited endocrine disorders
- Variants affecting potassium and sodium balance regulation
Who Should Consider This Test?
This genetic test is recommended for individuals experiencing:
- Early-onset hypertension resistant to conventional medications
- Unexplained hypokalemia (low potassium levels)
- Family history of hyperaldosteronism or endocrine disorders
- Adrenal gland abnormalities detected through imaging
- Symptoms of mineralocorticoid excess
- Multiple family members with hypertension or adrenal issues
Clinical Benefits of Genetic Testing
Undergoing the KCNJ5 genetic test provides numerous advantages:
- Accurate Diagnosis: Confirms or rules out genetic causes of hyperaldosteronism
- Personalized Treatment: Guides targeted therapy based on genetic findings
- Family Planning: Helps assess inheritance risk for future generations
- Early Intervention: Enables proactive management before complications develop
- Comprehensive Care: Integrates with multidisciplinary treatment approaches
Understanding Your Test Results
Your genetic test results will be carefully interpreted by our expert genetic counselors:
- Positive Result: Indicates presence of KCNJ5 mutation, confirming genetic predisposition to hyperaldosteronism type 3
- Negative Result: Suggests absence of tested mutations, though other genetic or environmental factors may contribute to symptoms
- Variant of Uncertain Significance: Requires additional clinical correlation and possibly family member testing
All results include detailed explanations and recommendations for next steps in your healthcare journey.
Test Pricing Information
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Accessibility
We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more cities. Our network of certified genetic testing facilities ensures you receive the same high-quality service regardless of location.
Take Control of Your Health Today
Don’t let uncertainty about your genetic health hold you back. Our comprehensive KCNJ5 genetic testing provides the clarity you need to make informed healthcare decisions. With results available in 3-4 weeks and sample collection options including blood, extracted DNA, or FTA card blood spots, getting tested has never been more convenient.
Ready to begin your genetic health journey? Book your KCNJ5 Gene Hyperaldosteronism Type 3 NGS Genetic DNA Test today by calling our dedicated healthcare line at +1(267) 388-9828 or schedule your appointment online. Our genetic counselors are available to answer your questions and guide you through the testing process.
