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CLCN5 Gene Hypophosphatemic Rickets NGS Genetic DNA Test

Original price was: R9,350.Current price is: R6,700.

-28%

Living with unexplained bone pain or family history of rickets can be worrying. Our CLCN5 Gene Hypophosphatemic Rickets NGS Genetic DNA Test provides the answers you need for just ZAR 6,700. This comprehensive test uses advanced NGS technology to detect mutations in the CLCN5 gene, which causes X-linked hypophosphatemic rickets. Early detection is crucial for preventing permanent bone deformities and growth issues in children. Our test includes professional genetic counselling to help you understand your family’s risk patterns. With results available in 3-4 weeks and nationwide coverage including Johannesburg, Cape Town, and Durban, you can trust Oracle Genomics for accurate, reliable genetic testing that puts your family’s health first.

📞 24/7 South African Support Team Call : +27 6412 56421

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
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CLCN5 Gene Rickets DNA Test | ZAR 6
CLCN5 Gene Hypophosphatemic Rickets NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Answers for Unexplained Bone Conditions with CLCN5 Gene Testing

When your child experiences persistent bone pain, delayed growth, or dental problems that doctors can’t explain, the uncertainty can be overwhelming. At Oracle Genomics, we understand the emotional toll of searching for answers about hereditary bone disorders. Our CLCN5 Gene Hypophosphatemic Rickets NGS Genetic DNA Test provides the clarity you need to make informed decisions about your family’s health.

Understanding the CLCN5 Gene Test

The CLCN5 gene plays a crucial role in kidney function and phosphate regulation in your body. When this gene has mutations, it can lead to X-linked hypophosphatemic rickets – a condition that affects bone development and causes phosphate to be improperly processed. Our advanced Next-Generation Sequencing (NGS) technology examines your DNA to identify any abnormalities in the CLCN5 gene, giving you definitive answers about this hereditary condition.

This isn’t just a simple blood test; it’s a comprehensive genetic analysis that provides lifelong insights into your family’s health patterns.

Who Should Consider This Test?

This test is particularly important if you or your family members experience:

  • Unexplained bone pain or tenderness in children
  • Delayed growth or short stature despite normal nutrition
  • Dental abscesses or early tooth decay without obvious cause
  • Bone deformities like bowed legs or knock knees
  • Family history of rickets or bone disorders
  • Previous abnormal blood tests showing low phosphate levels

If multiple family members across generations have shown similar symptoms, genetic testing becomes even more critical for accurate diagnosis and treatment planning.

Why Early Detection Matters for Your Family’s Health

Identifying CLCN5 gene mutations early can transform your family’s health outcomes:

  • Prevent Permanent Damage: Early treatment can prevent irreversible bone deformities in children
  • Targeted Treatment: Accurate diagnosis leads to specific phosphate and vitamin D therapy
  • Family Planning Insights: Understand inheritance patterns for future family decisions
  • Peace of Mind: End the uncertainty and get definitive answers about your symptoms
  • Cost Savings: Early intervention reduces long-term medical expenses and hospital visits

Understanding Your Test Results

We know waiting for genetic test results can be anxiety-provoking. That’s why we provide comprehensive support throughout the process:

  • Clear Reporting: Your results will be explained in easy-to-understand language
  • Genetic Counselling: Included professional session to discuss implications
  • Family Pedigree: Visual chart showing inheritance patterns in your family
  • Next Steps Guidance: Clear recommendations for treatment and monitoring
  • Ongoing Support: Access to our genetic specialists for follow-up questions

Whether your results show a mutation or provide reassuring clarity, you’ll have the professional guidance needed to move forward confidently.

Transparent Pricing – Investing in Your Family’s Health

Service Regular Price Special Price Savings
CLCN5 Gene Hypophosphatemic Rickets NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Your investment includes: Comprehensive genetic analysis, professional genetic counselling session, detailed results report, family pedigree chart, and ongoing specialist support.

Consider this: The cost of untreated rickets can include multiple specialist visits, dental procedures, and potential surgical corrections that far exceed the test price. Early detection is the most cost-effective approach to managing hereditary bone conditions.

Why South Africans Trust Oracle Genomics

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Tests supervised by qualified genetic specialists and physicians
  • Advanced Technology: State-of-the-art NGS technology for maximum accuracy
  • Rapid Turnaround: Results typically available within 3-4 weeks
  • Multiple Sample Options: Blood, extracted DNA, or simple FTA card blood drop
  • Comprehensive Preparation: Includes clinical history assessment and genetic counselling

Take Control of Your Family’s Bone Health Today

Don’t let uncertainty about hereditary bone conditions continue to worry you. With our special pricing of ZAR 6,700, there’s never been a better time to get the answers you deserve.

Limited Time Offer: This special pricing won’t last forever. Book your test now to secure your family’s health future.



Convenient Nationwide Access: Whether you’re in Johannesburg, Cape Town, Durban or anywhere in South Africa, we make genetic testing accessible and stress-free.