Find Answers for Unexplained Low Magnesium Levels
If you or your family members struggle with persistent magnesium deficiency despite supplementation, or face recurrent kidney stones and unexplained kidney issues, you’re not alone. Our CLDN16 Gene Hypomagnesemia Type 3 test provides the genetic clarity you need to understand your condition and take control of your health journey.
Understanding Your CLDN16 Gene Test
This advanced Next-Generation Sequencing (NGS) test examines your CLDN16 gene, which plays a crucial role in magnesium absorption in your kidneys. When this gene has mutations, it can lead to Hypomagnesemia Type 3 – a condition where your body struggles to retain magnesium, often accompanied by excessive calcium in urine and potential kidney damage.
Think of the CLDN16 gene as the gatekeeper for magnesium in your kidneys. When this gatekeeper isn’t working properly, valuable magnesium escapes through your urine, leaving your body deficient despite adequate intake.
Who Should Consider This Genetic Test?
This test is particularly important if you experience:
- Persistent low magnesium levels despite supplementation
- Recurrent kidney stones or urinary tract issues
- Family history of kidney problems or magnesium deficiency
- Unexplained muscle cramps, weakness, or fatigue
- Developmental delays in children with electrolyte imbalances
- Multiple family members with similar kidney or magnesium issues
Many South African families have found answers through genetic testing when traditional medical approaches couldn’t explain their persistent symptoms.
Why Early Detection Matters for Your Health
Identifying CLDN16 gene mutations early can significantly impact your long-term health outcomes:
- Prevent Kidney Damage: Early intervention can protect your kidneys from progressive damage
- Personalised Treatment: Receive targeted treatment strategies based on your genetic profile
- Family Planning: Understand inheritance patterns for future family planning decisions
- Peace of Mind: End the uncertainty and frustration of unexplained symptoms
- Cost Savings: Avoid repeated doctor visits and ineffective treatments
Understanding Your Test Results
We make understanding your results straightforward and reassuring:
- Clear Explanation: Your results come with easy-to-understand interpretations
- Genetic Counselling: Included session to discuss results and implications
- Family Pedigree: We help map your family history to understand inheritance patterns
- Next Steps Guidance: Clear recommendations for managing your condition
- Ongoing Support: Access to resources and support for your health journey
Remember, a positive result doesn’t mean certain illness – it means empowered prevention and management.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| CLDN16 Gene Hypomagnesemia Type 3 Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Includes genetic counselling, family pedigree analysis, and comprehensive results interpretation | |||
Consider this investment in your health compared to the potential costs of untreated kidney complications or repeated specialist consultations.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available across South Africa – Johannesburg, Cape Town, Durban, Pretoria and beyond
- Advanced Technology: State-of-the-art NGS testing for maximum accuracy
- Expert Team: Genetic specialists with years of experience
- Multiple Sample Options: Blood draw, extracted DNA, or simple FTA card
- Quick Turnaround: Results within 3-4 weeks
- Complete Privacy: Your genetic information is protected and confidential
Take the First Step Toward Clarity Today
Don’t let unexplained symptoms control your life. With our special pricing of ZAR 6,700, now is the perfect time to get the answers you deserve.
Limited Time Offer: This special pricing of ZAR 6,700 won’t last forever. Secure your test today and start your journey to better health understanding.
Ready to understand your genetic blueprint? Contact us today or book online for convenient testing across South Africa.
