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TCTN1 Gene Joubert Syndrome Type 13 NGS Genetic DNA Test

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

-28%

Facing concerns about Joubert Syndrome in your family? Our TCTN1 Gene Joubert Syndrome Type 13 NGS Genetic DNA Test provides the clarity you need for just ZAR 6,700. This comprehensive test uses advanced Next Generation Sequencing technology to detect mutations in the TCTN1 gene, offering life-changing insights for families affected by this rare neurological condition. With professional genetic counselling included, you’ll receive expert guidance on understanding your results and making informed health decisions. Available nationwide across South Africa, including Johannesburg, Cape Town, and Durban, our test delivers accurate, reliable results within 3-4 weeks. Take control of your family’s health journey 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

TCTN1 Joubert Syndrome DNA Test | ZAR 6
TCTN1 Gene Joubert Syndrome Type 13 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 neurological conditions affect your family, the uncertainty can be overwhelming. Our TCTN1 Gene Joubert Syndrome Type 13 NGS Genetic DNA Test provides the answers you need to make informed decisions about your family’s health journey. For just ZAR 6,700, gain access to cutting-edge genetic technology and professional support that brings peace of mind to families across South Africa.

Understanding the TCTN1 Joubert Syndrome Test

Joubert Syndrome Type 13 is a rare neurological disorder that affects brain development, and the TCTN1 gene plays a crucial role in this condition. Our test uses Next Generation Sequencing (NGS) technology – the gold standard in genetic testing – to thoroughly examine the TCTN1 gene for any mutations that could indicate Joubert Syndrome. This isn’t just a simple test; it’s a comprehensive analysis that provides the clarity families need when facing complex neurological concerns.

Who Should Consider This Test?

This test is specifically designed for individuals and families who are experiencing:

  • Children showing developmental delays or unusual eye movements
  • Family history of Joubert Syndrome or similar neurological conditions
  • Unexplained breathing pattern abnormalities in infants
  • Coordination difficulties or balance problems
  • Previous inconclusive neurological evaluations
  • Planning for pregnancy with family history of genetic disorders

If you’re in Johannesburg, Cape Town, Durban, or anywhere across South Africa and have concerns about neurological development in your family, this test provides the answers you’ve been searching for.

Why This Test Matters for Your Family’s Health

Early detection through genetic testing can be life-changing for families affected by Joubert Syndrome. By identifying the TCTN1 gene mutation early, you can:

  • Access appropriate medical care and interventions sooner
  • Make informed family planning decisions
  • Connect with specialist healthcare providers
  • Understand the inheritance pattern for future generations
  • Reduce anxiety through definitive answers
  • Participate in relevant clinical trials and support networks

Understanding Your Results with Professional Support

We understand that genetic test results can be overwhelming. That’s why every test includes a comprehensive genetic counselling session where our specialists will:

  • Create a detailed family pedigree chart to understand inheritance patterns
  • Explain your results in clear, understandable language
  • Discuss what the findings mean for your family’s health
  • Provide guidance on next steps and available resources
  • Connect you with appropriate medical specialists if needed

Your results will be available within 3-4 weeks, and our team will be with you every step of the way.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price
TCTN1 Joubert Syndrome DNA Test ZAR 9,350 ZAR 6,700
Includes: Genetic Counselling Session ✓ Included
Includes: Family Pedigree Analysis ✓ Included
Turnaround Time 3-4 Weeks

Considering the potential lifetime healthcare costs of undiagnosed conditions, this test represents significant value and peace of mind for your family.

Why Trust Oracle Genomics?

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

  • Nationwide Coverage – Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise – Working with qualified neurologists and genetic specialists
  • Advanced Technology – Using NGS technology for maximum accuracy
  • Patient-First Approach – Empathetic support throughout your journey
  • Proven Track Record – Thousands of satisfied families served

Take the First Step Toward Clarity Today

Don’t let uncertainty about neurological conditions control your family’s future. With convenient testing locations across South Africa and comprehensive support included, there’s no reason to wait.

Limited Time Offer: Book this week and secure your special pricing of ZAR 6,700 (regularly ZAR 9,350). Sample collection is simple – just a small blood sample or extracted DNA, with options available throughout South Africa.