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CC2D2A Gene Joubert Syndrome Type 9 NGS Genetic DNA Test

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

-28%

Facing concerns about Joubert Syndrome in your family? Our CC2D2A Gene Joubert Syndrome Type 9 NGS Genetic DNA Test provides the clarity you need for just ZAR 6,700. This comprehensive genetic analysis uses advanced NGS technology to detect mutations in the CC2D2A gene, which is crucial for proper brain development. If you’re experiencing developmental delays, abnormal eye movements, or breathing difficulties, this test can provide definitive answers. Early detection through genetic testing allows for better management of symptoms and informed family planning decisions. Our test is conducted with the highest accuracy standards, giving you reliable results within 3-4 weeks. With nationwide coverage across South Africa including Johannesburg, Cape Town, Durban, and Pretoria, accessing this vital genetic testing has never been easier. Take control of your family’s health journey today with confidence and peace of mind.

📞 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

CC2D2A Joubert Syndrome DNA Test | ZAR 6
CC2D2A Gene Joubert Syndrome Type 9 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity for Joubert Syndrome Concerns with Advanced Genetic Testing

When you’re worried about developmental delays or neurological symptoms in your child, the uncertainty can be overwhelming. Our CC2D2A Gene Joubert Syndrome Type 9 NGS Genetic DNA Test provides the answers you need to move forward with confidence. For just ZAR 6,700, you can access cutting-edge genetic analysis that brings peace of mind and clear direction for your family’s health journey.

Understanding the CC2D2A Joubert Syndrome Test

The CC2D2A gene plays a critical role in brain development, specifically in the formation of the cerebellar vermis – the part of the brain responsible for coordination and balance. When mutations occur in this gene, it can lead to Joubert Syndrome Type 9, a rare neurological disorder. Our test uses Next-Generation Sequencing (NGS) technology to thoroughly examine the CC2D2A gene, identifying any abnormalities with exceptional accuracy.

This isn’t just another medical test – it’s a comprehensive genetic analysis that provides definitive answers about your child’s neurological health. The process is straightforward and conducted with the utmost care and professionalism by our experienced neurological genetics team.

Who Should Consider This Genetic Test?

This test is particularly important if you or your child are experiencing:

  • Developmental delays in motor skills or speech
  • Abnormal eye movements (nystagmus) or vision problems
  • Breathing difficulties or irregular breathing patterns
  • Poor muscle coordination and balance issues
  • Intellectual disability or learning challenges
  • Family history of Joubert Syndrome or similar neurological conditions

If you’re planning a family and have concerns about genetic risks, this test can provide valuable insights for informed decision-making.

Why Early Detection Matters for Your Family’s Health

Getting a definitive diagnosis through genetic testing offers numerous life-changing benefits:

  • Early Intervention: Identify conditions early to access appropriate therapies and support services
  • Treatment Planning: Work with healthcare providers to create targeted treatment strategies
  • Family Planning: Make informed decisions about future pregnancies with genetic counselling
  • Peace of Mind: Reduce uncertainty and anxiety with clear, accurate results
  • Medical Management: Coordinate care with specialists who understand your specific condition

Early detection can significantly improve quality of life and help families access the right support systems at the right time.

Understanding Your Test Results

We understand that waiting for genetic test results can be stressful. That’s why we provide comprehensive support throughout the process:

  • Clear Interpretation: Your results will be explained in easy-to-understand language
  • Genetic Counselling: Included session to help you understand the implications
  • Medical Guidance: Recommendations for next steps and specialist referrals
  • Family Support: Information about support groups and resources

Our team is here to ensure you feel supported and informed every step of the way, from testing to treatment planning.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price
CC2D2A Joubert Syndrome NGS Test ZAR 9,350 ZAR 6,700
Genetic Counselling Session Included
Family Pedigree Analysis Included
Results Interpretation Included

Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card

Considering the lifelong impact of early diagnosis, this test represents exceptional value for your family’s health investment.

Why Trust Oracle Genomics?

We’ve built our reputation on accuracy, compassion, and professional excellence:

  • Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Expert Team: Specialised neurologists and genetic counsellors with extensive experience
  • Advanced Technology: State-of-the-art NGS technology for unparalleled accuracy
  • Patient-Focused Care: Empathetic support throughout your testing journey
  • Proven Track Record: Trusted by families and healthcare providers nationwide

Your family’s health deserves the highest standard of care – and that’s exactly what we deliver.

Take the First Step Toward Clarity Today

Don’t let uncertainty about neurological symptoms control your family’s future. With our special pricing of ZAR 6,700, there’s never been a better time to get the answers you need.

Limited Time Offer: This special pricing won’t last forever. Secure your family’s peace of mind while you can still save ZAR 2,650.

Available at our centres in Johannesburg, Cape Town, Durban, Pretoria and nationwide. Your journey to clarity starts with one simple decision.