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PDE6D Gene Joubert Syndrome Type 22 NGS Genetic DNA Test

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

-28%

Facing concerns about Joubert Syndrome Type 22 in your family? Our advanced PDE6D gene testing provides the clarity you need. Using cutting-edge NGS technology, this comprehensive DNA analysis detects the specific genetic mutations responsible for Joubert Syndrome Type 22, offering you definitive answers and peace of mind. For just ZAR 6,700 (regularly ZAR 9,350), you’ll receive accurate, reliable results within 3-4 weeks. Our test is particularly crucial for families with neurological development concerns, unexplained coordination difficulties, or breathing pattern abnormalities in infants. With nationwide coverage across South Africa including Johannesburg, Cape Town, Durban and Pretoria, we make genetic testing accessible and trustworthy. Take control of your family’s health journey with confidence in our medical expertise and commitment to accuracy.

📞 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

Joubert Syndrome Type 22 DNA Test | ZAR 6
PDE6D Gene Joubert Syndrome Type 22 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity About Joubert Syndrome Type 22 in Your Family

When neurological concerns affect your child or family members, the uncertainty can be overwhelming. Our PDE6D Gene Joubert Syndrome Type 22 NGS Genetic DNA Test provides the definitive answers you need to make informed healthcare decisions and plan for the future with confidence.

Understanding the PDE6D Gene Joubert Syndrome Test

Joubert Syndrome Type 22 is a rare neurological disorder that affects brain development, particularly the cerebellum and brainstem. Our advanced Next-Generation Sequencing (NGS) technology examines the PDE6D gene with exceptional precision, identifying specific genetic mutations that cause this condition. This isn’t just a test – it’s a pathway to understanding your family’s genetic health.

The test requires only a simple blood sample or extracted DNA, making the process straightforward and minimally invasive. With results available in 3-4 weeks, you won’t face prolonged uncertainty about your family’s health situation.

Who Should Consider This Genetic Test?

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

  • Unexplained developmental delays in infants or children
  • Abnormal eye movements or vision problems
  • Breathing pattern abnormalities, especially in newborns
  • Coordination difficulties or balance problems
  • Family history of neurological disorders
  • Previous children with Joubert Syndrome symptoms

Early detection through genetic testing can significantly improve management strategies and quality of life outcomes.

Why Early Detection Matters for Your Family’s Health

Knowing your genetic status provides numerous benefits:

  • Peace of Mind: Eliminate uncertainty and reduce anxiety about your family’s health future
  • Early Intervention: Access appropriate therapies and support services sooner
  • Family Planning: Make informed decisions about future pregnancies
  • Personalised Care: Develop targeted healthcare plans based on accurate genetic information
  • Medical Preparedness: Anticipate and manage potential health challenges effectively

Understanding Your Test Results

We understand that waiting for genetic test results can be stressful. Our comprehensive reporting includes:

  • Clear, easy-to-understand explanations of your genetic findings
  • Detailed interpretation by our expert neurologists and genetic specialists
  • Personalised recommendations for next steps and management options
  • Access to genetic counselling to help you understand the implications
  • Ongoing support for your healthcare journey

Remember: Knowledge is power, and understanding your genetic makeup empowers you to take control of your health.

Affordable, Accessible Genetic Testing

Test Option Regular Price Special Price Savings
PDE6D Gene Joubert Syndrome Type 22 NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Includes comprehensive genetic analysis, expert interpretation, and detailed reporting

Why Trust Oracle Genomics?

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
  • Advanced Technology: State-of-the-art NGS technology ensuring 99.9% accuracy
  • Genetic Counselling: Pre-test counselling to create your family pedigree chart
  • Confidential Service: Your genetic information is protected with strict privacy protocols
  • Proven Track Record: Thousands of South African families trust our genetic testing services

Take the First Step Toward Genetic Clarity

Don’t let uncertainty about Joubert Syndrome Type 22 create unnecessary stress in your family. Our genetic testing provides the answers you need to move forward with confidence.

Multiple Ways to Book Your Test:

  • Online Booking: Secure, confidential online scheduling available 24/7
  • Telephone Consultation: Speak directly with our genetic specialists
  • In-Person Visit: Visit our conveniently located centres nationwide

Limited Time Special: Save ZAR 2,650 on your genetic testing. Early detection can make a significant difference in management outcomes.

Convenient Sample Collection: Choose from blood draw, extracted DNA, or simple FTA card blood spot collection.


Your journey to genetic clarity starts here. Trust Oracle Genomics for accurate, compassionate genetic testing that puts your family’s health first.