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CYP2R1 Gene Rickets Vitamin D 25-Hydroxylation-Deficient Type 1B NGS Genetic DNA Test

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

-28%

If you or your child are experiencing bone pain, muscle weakness, or delayed growth that might indicate vitamin D deficiency rickets, our CYP2R1 gene test provides the definitive answers you need. This comprehensive NGS genetic DNA test specifically identifies mutations in the CYP2R1 gene that cause vitamin D 25-hydroxylation-deficient type 1B rickets. For just ZAR 6,700 (regularly ZAR 9,350), you’ll receive precise genetic analysis that can guide proper treatment and prevent long-term complications. Our test includes professional genetic counselling to help you understand your family’s risk patterns and create a personalised health management plan. With results in 3-4 weeks and nationwide coverage across South Africa, 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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CYP2R1 Rickets DNA Test | ZAR 6
CYP2R1 Gene Rickets Vitamin D 25-Hydroxylation-Deficient Type 1B NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity for Bone Health Concerns with CYP2R1 Gene Testing

When you’re worried about unexplained bone pain, muscle weakness, or growth delays in your child, the uncertainty can be overwhelming. Our CYP2R1 gene test provides the definitive answers you need to understand whether vitamin D metabolism issues are affecting your family’s health. For South African families seeking clarity about hereditary rickets conditions, this advanced genetic analysis offers peace of mind and a clear path forward.

Understanding Your CYP2R1 Genetic Test

The CYP2R1 gene plays a crucial role in converting vitamin D into its active form that your body can use. When this gene has mutations, it can lead to vitamin D 25-hydroxylation-deficient type 1B rickets – a condition where vitamin D supplements alone may not be effective because your body can’t properly process them. Our Next Generation Sequencing (NGS) technology examines your CYP2R1 gene with exceptional accuracy, identifying specific mutations that could be causing your symptoms.

Who Should Consider This Genetic Test?

This test is particularly important if you or your child experience:

  • Unexplained bone pain or tenderness
  • Muscle weakness that doesn’t improve with exercise
  • Delayed growth or short stature in children
  • Bone deformities or bowing of legs
  • Dental problems or delayed tooth development
  • Family history of rickets or vitamin D resistance
  • Poor response to standard vitamin D treatment

Many South African families struggle with these symptoms without understanding the underlying genetic cause. Early genetic testing can prevent years of ineffective treatments and unnecessary suffering.

Why This Test Matters for Your Family’s Health

Getting the right diagnosis means getting the right treatment. When we identify CYP2R1 gene mutations, we can:

  • Guide you toward effective treatment options specifically for your genetic condition
  • Prevent long-term bone damage and deformities through early intervention
  • Provide clarity about inheritance patterns for family planning decisions
  • Eliminate the frustration of trying treatments that won’t work for your specific condition
  • Offer peace of mind through definitive answers about your health concerns

Understanding Your Test Results

We know waiting for genetic test results can be anxiety-provoking. That’s why we include comprehensive genetic counselling with every test. Our specialists will:

  • Explain your results in clear, understandable language
  • Create a family pedigree chart to show inheritance patterns
  • Discuss what your results mean for your health management
  • Provide guidance on next steps and treatment options
  • Answer all your questions with patience and expertise

Your results will clearly indicate whether CYP2R1 gene mutations are present and what that means for your vitamin D metabolism.

Transparent Pricing – No Hidden Costs

Service Regular Price Special Price
CYP2R1 Gene NGS Test ZAR 9,350 ZAR 6,700
Genetic Counselling Session INCLUDED
Family Pedigree Analysis INCLUDED
Results Interpretation INCLUDED

Consider the long-term savings: Early diagnosis can prevent costly treatments for bone deformities and chronic pain management.

Why Trust Oracle Genomics?

We understand that genetic testing requires absolute confidence in accuracy and professionalism. That’s why we:

  • Use advanced NGS technology for 99.9% accuracy in mutation detection
  • Employ certified genetic counsellors who specialise in metabolic disorders
  • Offer nationwide coverage with testing centres in Johannesburg, Cape Town, Durban, and Pretoria
  • Maintain strict confidentiality and ethical standards
  • Provide clear, compassionate communication throughout your testing journey

Turnaround Time: 3-4 weeks from sample receipt
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Preparation: Bring clinical history and be ready for genetic counselling session

Take Control of Your Bone Health Today

Don’t let uncertainty about vitamin D metabolism issues continue to affect your quality of 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 (regularly ZAR 9,350) includes complete genetic counselling and family analysis. Book now to secure your spot.

Available at our centres in Johannesburg, Cape Town, Durban, Pretoria and nationwide through our partner network.