Find Answers for Unexplained Magnesium Deficiency and Kidney Issues
When your body struggles to maintain proper magnesium levels despite treatment, it can feel frustrating and concerning. The CLDN19 Gene Hypomagnesemia Type 5 NGS Genetic DNA Test provides the clarity you need to understand the genetic root cause of your symptoms and take control of your health journey.
Understanding Your CLDN19 Gene Test
This advanced genetic test examines the CLDN19 gene, which plays a crucial role in maintaining magnesium balance in your body. When this gene has mutations, it can lead to Hypomagnesemia Type 5 – a condition where your kidneys cannot properly reabsorb magnesium, causing it to be lost through urine. Our NGS (Next Generation Sequencing) technology provides the most accurate analysis available, giving you reliable results you can trust for making important health decisions.
Who Should Consider This Genetic Test?
This test is particularly important if you or your family members experience:
- Persistent low magnesium levels despite supplementation
- Unexplained kidney function issues or kidney stones
- Neurological symptoms like muscle weakness or tremors
- Family history of magnesium deficiency disorders
- Vision problems or eye abnormalities
- Developmental delays in children
Early detection can prevent serious complications and help guide appropriate treatment strategies.
Why Early Detection Matters for Your Health
Identifying CLDN19 gene mutations early provides significant benefits:
- Prevent Kidney Damage: Early intervention can protect your kidneys from long-term damage
- Proper Treatment Planning: Accurate diagnosis guides effective magnesium replacement therapy
- Family Planning Insights: Understand inheritance patterns for future family planning
- Peace of Mind: End the uncertainty and get clear answers about your health condition
- Comprehensive Care: Coordinate with specialists for optimal management
Understanding Your Test Results
Our genetic counselling team will carefully explain your results in clear, understandable language. We’ll help you understand what any identified mutations mean for your health and provide guidance on next steps. Whether your results show a positive finding or rule out CLDN19-related conditions, you’ll receive the support and information needed to make informed decisions about your healthcare.
Transparent Pricing and Value
| Service | Regular Price | Special Price |
|---|---|---|
| CLDN19 Gene Hypomagnesemia Type 5 NGS Test | ZAR 6,700 |
Your investment includes: Comprehensive genetic analysis, genetic counselling session, detailed results interpretation, and ongoing support. Considering the potential savings from preventing serious kidney complications, this test represents excellent value for your long-term health.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Advanced Technology: State-of-the-art NGS testing for maximum accuracy
- Professional Expertise: Genetic counsellors and medical specialists
- Quick Turnaround: Results in 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple FTA card blood drop
- Comprehensive Preparation: Clinical history review and family pedigree analysis included
Take the First Step Toward Clarity
Don’t let unexplained symptoms control your life. Early detection of CLDN19 gene mutations can prevent serious health complications and provide the answers you need for proper management. Our team is ready to support you through every step of the testing process.
Limited Time Offer: Save ZAR 2,650 on your genetic testing. Contact us today to schedule your appointment in Johannesburg, Cape Town, Durban, or Pretoria.
