Sale!

RIN2 Gene Macrocephaly Alopecia Cutis Laxa and Scoliosis NGS Genetic DNA Test

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

-28%

If you’re concerned about rare genetic conditions affecting your child’s development, our RIN2 Gene Macrocephaly Alopecia Cutis Laxa and Scoliosis NGS Genetic DNA Test provides the answers you need. For only ZAR 6,700, this comprehensive test uses advanced Next Generation Sequencing technology to detect mutations in the RIN2 gene associated with these complex conditions. We understand the anxiety that comes with unexplained symptoms, which is why our test offers clarity and peace of mind. With genetic counselling included and nationwide coverage across South Africa, including Johannesburg, Cape Town, and Durban, we make professional genetic testing accessible and trustworthy. Early detection can guide appropriate management and treatment strategies, giving your family the confidence to make informed healthcare decisions.

📞 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

RIN2 Gene Test ZAR 6
RIN2 Gene Macrocephaly Alopecia Cutis Laxa and Scoliosis NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

[wpforms id=”1190″ title=”true” description=”Request a call back”]

Find Clarity for Your Child’s Health Journey

When your child shows unusual symptoms like an enlarged head, hair loss, loose skin, or spinal curvature, the uncertainty can be overwhelming. Our RIN2 Gene Test provides the answers you’ve been searching for, using cutting-edge technology to detect rare genetic conditions that affect development and quality of life.

Understanding the RIN2 Gene Test

The RIN2 Gene Macrocephaly Alopecia Cutis Laxa and Scoliosis NGS Genetic DNA Test is a sophisticated diagnostic tool that examines the RIN2 gene for mutations associated with a rare genetic syndrome. Using Next Generation Sequencing (NGS) technology, we can identify specific genetic variations that may be causing your child’s symptoms, providing crucial information for their healthcare journey.

This test is particularly important because RIN2-related disorders can present with multiple symptoms that may seem unrelated, making accurate diagnosis challenging without genetic testing.

Who Should Consider This Test?

This test is recommended for children and individuals showing one or more of these concerning symptoms:

  • Macrocephaly (unusually large head circumference)
  • Alopecia (hair loss or thinning)
  • Cutis laxa (loose, sagging skin)
  • Scoliosis (abnormal spinal curvature)
  • Developmental delays or concerns
  • Family history of similar symptoms

If your child has been experiencing these symptoms without clear explanation, this test can provide the diagnostic clarity needed to guide appropriate care and management.

Why Early Detection Matters for Your Family

Getting an accurate diagnosis through genetic testing offers multiple benefits for your child’s health and your family’s peace of mind:

  • Personalised Treatment Plans: Knowing the specific genetic cause allows healthcare providers to create targeted management strategies
  • Early Intervention: Prompt diagnosis enables early intervention, which can significantly improve outcomes
  • Family Planning Guidance: Understanding the genetic basis helps with informed family planning decisions
  • Reduced Diagnostic Uncertainty: End the cycle of multiple doctor visits and unclear diagnoses
  • Access to Specialised Care: Connect with the right specialists and support networks

Understanding Your Results with Confidence

We understand that waiting for genetic test results can be anxiety-provoking. Our comprehensive approach includes:

  • Clear, Understandable Reports: Results presented in plain language with medical interpretation
  • Genetic Counselling Support: Professional guidance to help you understand what the results mean for your family
  • Follow-up Recommendations: Specific next steps based on your results
  • Ongoing Support: Access to our team for any questions after receiving results

Your results will clearly indicate whether RIN2 gene mutations were detected and what this means for your child’s health management.

Affordable, Accessible Genetic Testing

Test Feature Details Value
Regular Price ZAR 9,350 Comprehensive genetic analysis
Special Price ZAR 6,700 Limited time savings of ZAR 2,650
Turnaround Time 3-4 Weeks Timely results for prompt action
Sample Type Blood, Extracted DNA, or Blood on FTA Card Convenient collection options
Included Services Genetic Counselling & Clinical Assessment Complete diagnostic package

Consider the long-term value: Early diagnosis can prevent years of unnecessary treatments and specialist visits, making this test a valuable investment in your child’s health future.

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Specialised paediatric genetic testing with professional interpretation
  • Advanced Technology: State-of-the-art NGS technology for maximum accuracy
  • Patient-Centred Care: Empathetic support throughout your testing journey
  • Proven Accuracy: Reliable results you can trust for important healthcare decisions

Take the First Step Toward Clarity Today

Don’t let uncertainty about your child’s symptoms continue to cause worry. Our RIN2 Gene Test provides the answers you need to move forward with confidence.



Limited Time Offer: Save ZAR 2,650 on this comprehensive genetic test. Early detection can make a significant difference in your child’s development and quality of life.

“The peace of mind we gained from getting a clear diagnosis was priceless. We finally had answers and could focus on the right treatments.” – Satisfied Parent, Cape Town