Find Clarity for Unexplained Fatigue and Salt Cravings
When your body struggles to maintain proper salt and fluid balance, it can feel like you’re fighting an invisible battle. The CYP11B2 gene test offers definitive answers for congenital hypoaldosteronism – a condition that affects your body’s ability to produce aldosterone, the hormone that regulates salt and water balance.
Understanding Your CYP11B2 Gene Test
This advanced Next-Generation Sequencing (NGS) test examines your CYP11B2 gene to identify mutations that cause congenital hypoaldosteronism due to CMO I deficiency. Think of it as reading your body’s instruction manual to find the specific paragraph that needs correction. Our test provides the clarity you need to move from uncertainty to actionable health management.
Who Should Consider This Genetic Test?
This test is particularly important if you or your child experiences:
- Persistent fatigue that doesn’t improve with rest
- Unexplained salt cravings or excessive thirst
- Low blood pressure that causes dizziness
- Poor growth or development in children
- Family history of adrenal or hormonal disorders
- Unexplained electrolyte imbalances
Many South Africans live with these symptoms for years without understanding the underlying cause. This test provides the answers you deserve.
Why Early Detection Matters for Your Health
Identifying congenital hypoaldosteronism early can transform your quality of life. With proper diagnosis and treatment, you can:
- Manage symptoms effectively with targeted medication
- Prevent dangerous electrolyte imbalances
- Support normal growth and development in children
- Reduce the risk of adrenal crises
- Make informed family planning decisions
- Experience improved energy levels and overall wellbeing
Early detection means you can take control of your health journey rather than reacting to symptoms.
Understanding Your Test Results
We know waiting for genetic test results can be anxiety-provoking. That’s why we provide comprehensive genetic counselling before your test to prepare you for all possible outcomes. Your results will clearly indicate:
- Whether a CYP11B2 gene mutation is present
- The specific type of mutation detected
- What the results mean for your health management
- Recommended next steps and treatment options
- Family implications and testing recommendations
Our genetic counsellors will walk you through every step, ensuring you feel supported and informed throughout the process.
Transparent Pricing – Your Health Investment
| Service | Regular Price | Special Price |
|---|---|---|
| CYP11B2 Gene Test with Genetic Counselling | ZAR 6,700 |
Your investment includes:
- Comprehensive NGS genetic testing
- Professional genetic counselling session
- Family pedigree analysis
- Detailed results interpretation
- 3-4 week turnaround time
- Ongoing support and guidance
Why Trust Oracle Genomics?
As South Africa’s leading genetic testing provider, we combine medical excellence with compassionate care:
- Nationwide Coverage: Accessible testing in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Our endocrinology specialists understand the complexities of hormonal disorders
- Accuracy Guarantee: Advanced NGS technology ensures 99.9% detection accuracy
- Patient-First Approach: We prioritize your comfort and understanding throughout the process
- Convenient Sampling: Simple blood draw or FTA card options available
Take the First Step Toward Health Clarity
Don’t let unexplained symptoms control your life. Our CYP11B2 gene test provides the answers you need to take control of your health journey. With our special pricing of ZAR 6,700 and comprehensive genetic counselling included, there’s never been a better time to get the clarity you deserve.
Limited Time Offer: Book before the end of the month to secure your special pricing of ZAR 6,700 (regularly ZAR 9,350). Your health journey starts with one simple decision.
