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RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test

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

-28%

If you or your child are experiencing unusual bone development, delayed tooth eruption, or have a family history of skeletal abnormalities, our RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test provides the answers you need. For just ZAR 6,700 (regularly ZAR 9,350), this comprehensive test uses advanced Next-Generation Sequencing technology to deliver highly accurate results within 3-4 weeks. Our test is specifically designed to detect mutations in the RUNX2 gene, which is responsible for cleidocranial dysplasia – a condition affecting bone and tooth development. We include professional genetic counselling to help you understand your family history and create a comprehensive pedigree chart. With testing centres across South Africa including Johannesburg, Cape Town, and Durban, getting clarity about your genetic health has never been more accessible. Trust Oracle Genomics for reliable, professional genetic testing that puts your health concerns first.

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

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
Guaranteed Safe Checkout

RUNX2 Gene Cleidocranial Dysplasia DNA Test | ZAR 6
RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Cleidocranial Dysplasia: Your Path to Genetic Clarity

When you notice unusual bone development in yourself or your child, or experience delayed tooth eruption that doesn’t seem normal, it’s natural to feel concerned and seek answers. Our RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test is designed specifically to provide the clarity and peace of mind you deserve. Using state-of-the-art genetic technology, we help South African families understand their genetic health with confidence and accuracy.

What This Test Detects

This advanced genetic test specifically examines the RUNX2 gene, which plays a crucial role in bone and tooth development. When mutations occur in this gene, they can lead to cleidocranial dysplasia – a condition characterized by underdeveloped or absent collarbones, delayed closure of skull bones, and dental abnormalities. Our Next-Generation Sequencing (NGS) technology provides comprehensive analysis of this gene, ensuring we don’t miss any potential mutations that could be affecting your health.

Who Should Consider This Test

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

  • Unusually prominent forehead or wide-set eyes
  • Delayed loss of baby teeth or delayed eruption of adult teeth
  • Ability to bring shoulders unusually close together
  • Short stature compared to family members
  • Family history of skeletal development issues
  • Diagnosed bone abnormalities in childhood

Many South African families live with these symptoms without understanding their genetic cause, but early detection can make a significant difference in management and treatment planning.

Why Early Detection Matters for Your Health

Getting a definitive diagnosis through genetic testing provides numerous benefits:

  • Peace of Mind: Eliminate uncertainty about your or your child’s condition
  • Proper Management: Work with healthcare providers to create appropriate care plans
  • Family Planning: Understand inheritance patterns for future family decisions
  • Dental Care Planning: Prepare for specialized dental treatments that may be needed
  • Early Intervention: Address potential complications before they become serious

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. That’s why we provide:

  • Clear, Easy-to-Understand Reports: Your results will be explained in plain language
  • Professional Support: Access to genetic counselling to help interpret your results
  • Follow-up Guidance: Recommendations for next steps based on your specific results
  • Family Implications: Understanding what your results mean for other family members

Our team is committed to ensuring you feel supported and informed throughout the entire process.

Transparent Pricing – Excellent Value

Service Regular Price Special Price Savings
RUNX2 Gene Cleidocranial Dysplasia NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

What’s Included: Comprehensive genetic analysis, professional genetic counselling session, detailed results report, and ongoing support.

Turnaround Time: 3-4 weeks

Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card

Why Trust Oracle Genomics

As South Africa’s leading genetic testing provider, we offer:

  • Nationwide Coverage: Testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Working with qualified dermatologists and genetic specialists
  • Advanced Technology: Using Next-Generation Sequencing for maximum accuracy
  • Patient-Focused Care: We prioritize your comfort and understanding throughout the process
  • Proven Track Record: Thousands of South Africans trust us with their genetic health

Take Control of Your Genetic Health Today

Don’t let uncertainty about bone and dental development concerns continue to worry you. Our special pricing of ZAR 6,700 makes professional genetic testing more accessible than ever. With convenient locations across South Africa and comprehensive support throughout your testing journey, there’s no reason to delay getting the answers you need.

Multiple Ways to Book Your Test:

  • Online Booking: Secure your appointment through our website 24/7
  • Telephone Consultation: Speak directly with our genetic counselling team
  • In-Person Visit: Visit any of our nationwide testing centres

Limited Time Offer: This special pricing of ZAR 6,700 won’t last forever. Take advantage of our ZAR 2,650 savings and get the genetic clarity you deserve.

“Early detection through genetic testing gave our family the answers we needed to plan proper care. The peace of mind was priceless.” – Satisfied Oracle Genomics Patient