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EXOSC3 Gene Pontocerebellar Hypoplasia Type 1B NGS Genetic DNA Test

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

-28%

Facing concerns about neurological development in your child? Our EXOSC3 Gene Pontocerebellar Hypoplasia Type 1B NGS Genetic DNA Test provides definitive answers for families across South Africa. For just ZAR 6,700 (regularly ZAR 9,350), this advanced test uses Next Generation Sequencing technology to detect mutations in the EXOSC3 gene associated with this rare neurological condition. Early detection is crucial for managing symptoms and planning appropriate care strategies. Our test offers 99.9% accuracy and comprehensive genetic counselling to help you understand your results. With nationwide coverage including Johannesburg, Cape Town, and Durban, we make specialised genetic testing accessible to all South African families. Take the first step toward clarity and peace of mind with our trusted genetic testing services.

📞 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

EXOSC3 Gene PCH1B DNA Test | ZAR 6
EXOSC3 Gene Pontocerebellar Hypoplasia Type 1B NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity for Your Child’s Neurological Health

When you notice developmental delays or neurological symptoms in your child, the uncertainty can be overwhelming. Our EXOSC3 Gene Pontocerebellar Hypoplasia Type 1B NGS Genetic DNA Test provides the answers South African families need to make informed healthcare decisions. Using cutting-edge Next Generation Sequencing technology, we deliver accurate, reliable results that can guide treatment and care planning.

Understanding the EXOSC3 Gene Test

Pontocerebellar Hypoplasia Type 1B is a rare neurological disorder that affects brain development, particularly in the cerebellum and brainstem. Our test specifically examines the EXOSC3 gene for mutations that cause this condition. Unlike basic genetic tests, our NGS technology provides comprehensive analysis of the entire gene sequence, ensuring no potential mutations are missed.

The test is performed using a simple blood sample or extracted DNA, making it accessible for patients of all ages across South Africa. Our laboratory processes are validated to international standards, giving you confidence in every result.

Who Should Consider This Test?

This test is particularly important for families who have noticed:

  • Delayed motor development in infants and young children
  • Muscle weakness or poor muscle tone (hypotonia)
  • Feeding difficulties and breathing problems
  • Abnormal eye movements or vision issues
  • Family history of similar neurological conditions
  • Unexplained developmental regression

If your child is showing any of these symptoms, or if there’s a family history of neurological disorders, early testing can provide crucial information for their care team.

Why Early Detection Matters for Your Family

Getting a definitive diagnosis through genetic testing offers multiple benefits:

  • Accurate Diagnosis: Eliminate uncertainty and get clear answers about your child’s condition
  • Personalised Care Planning: Work with healthcare providers to develop targeted treatment strategies
  • Family Planning Guidance: Understand inheritance patterns for future family planning decisions
  • Early Intervention: Access appropriate therapies and support services sooner
  • Peace of Mind: Reduce the stress of not knowing and focus on providing the best care

Understanding Your Test Results

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

  • Clear Result Interpretation: Our reports are written in easy-to-understand language with clear explanations
  • Genetic Counselling: Every test includes a session with our qualified genetic counsellors
  • Family Pedigree Analysis: We help map your family history to understand inheritance patterns
  • Healthcare Provider Coordination: We work directly with your neurologist or paediatrician

Our turnaround time of 3-4 weeks ensures you get answers as quickly as possible without compromising accuracy.

Transparent Pricing – No Hidden Costs

Service Regular Price Special Price Savings
EXOSC3 Gene PCH1B NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Genetic Counselling Session Included at no extra cost
Family Pedigree Analysis Included at no extra cost
Result Interpretation Included at no extra cost

All prices include VAT and there are no hidden laboratory fees. Payment plans available upon request.

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Serving patients in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
  • Technology Leadership: Latest NGS technology ensuring 99.9% accuracy rates
  • Patient-Centred Care: Empathetic support throughout your testing journey
  • International Standards: Laboratory accredited to global quality standards

Take the First Step Toward Answers Today

Don’t let uncertainty about your child’s neurological health continue. Our EXOSC3 Gene test provides the clarity you need to make the best decisions for your family’s future.

Easy Booking Options:

  • Online Booking: Schedule your test through our secure portal
  • Telephone Consultation: Speak directly with our genetic counsellors
  • Referral Pathway: Ask your healthcare provider to refer you
  • Mobile Services: Home sample collection available in major centres

Limited Time Offer: Save ZAR 2,650 on your genetic testing. Early detection can make a significant difference in management outcomes. Book your test today and take control of your family’s neurological health journey.

Ready to Get Started? Contact our genetic counselling team today at [Phone Number] or visit our website to schedule your consultation. We’re here to support you every step of the way.