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PLCB4 Gene Auriculocondylar Syndrome Type 2 NGS Genetic DNA Test

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

-28%

Facing concerns about Auriculocondylar Syndrome Type 2 in your family? Our comprehensive PLCB4 Gene NGS Genetic DNA Test provides the answers you need for peace of mind. For only ZAR 6,700 (regularly ZAR 9,350), this advanced test uses Next Generation Sequencing technology to deliver highly accurate results within 3-4 weeks. We understand the anxiety that comes with genetic conditions, which is why we include essential genetic counselling to help you understand your family’s health patterns. Our test is specifically designed for South African families seeking clarity about this rare genetic disorder. With nationwide coverage including Johannesburg, Cape Town, and Durban, accessing expert genetic testing has never been easier. Trust Oracle Genomics for reliable, compassionate care that puts your family’s health first.

📞 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

PLCB4 Gene Test ZAR 6
PLCB4 Gene Auriculocondylar Syndrome Type 2 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding PLCB4 Gene Auriculocondylar Syndrome Type 2: Your Path to Clarity

When you’re concerned about genetic conditions affecting your child’s development, the uncertainty can be overwhelming. Auriculocondylar Syndrome Type 2 is a rare genetic disorder that affects facial and ear development, and we understand the emotional journey families face when seeking answers. At Oracle Genomics, we provide the clarity and confidence you need through our advanced PLCB4 Gene NGS Genetic DNA Test.

What This Test Detects: Clear Answers for Complex Questions

The PLCB4 Gene test specifically identifies mutations in the PLCB4 gene, which is responsible for Auriculocondylar Syndrome Type 2. This condition affects the development of ears and jaw, and our test provides definitive answers about whether this genetic variation is present. Using Next Generation Sequencing (NGS) technology, we examine the entire PLCB4 gene with exceptional accuracy, giving you reliable results you can trust for making informed healthcare decisions.

Who Should Consider This Important Genetic Test?

This test is particularly important for families experiencing:

  • Children with unusual ear shape or positioning
  • Facial asymmetry or jaw development concerns
  • Family history of craniofacial abnormalities
  • Unexplained developmental delays in facial features
  • Suspected genetic syndromes affecting ear and jaw formation

If you’ve noticed these symptoms in your child or have family members with similar concerns, this test can provide the answers that help guide appropriate medical care and interventions.

Why Early Detection Matters for Your Child’s Future

Getting clear genetic answers early can significantly impact your child’s health journey:

  • Early Intervention Planning: Knowing the genetic cause allows for timely medical and therapeutic interventions
  • Family Planning Guidance: Understand inheritance patterns for future family decisions
  • Reduced Diagnostic Uncertainty: End the cycle of unanswered questions and multiple specialist visits
  • Personalised Care Pathways: Enable targeted treatments and management strategies
  • Peace of Mind: Replace anxiety with actionable information and clear next steps

Understanding Your Results: Clear Guidance Every Step

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

  • Genetic Counselling Included: Every test includes professional genetic counselling to help interpret results and understand family implications
  • Clear Result Interpretation: Results are presented in easy-to-understand language with medical guidance
  • Family Pedigree Analysis: We help map your family history to understand inheritance patterns
  • Next Steps Guidance: Clear recommendations for medical follow-up and specialist referrals
  • Ongoing Support: Access to our genetic specialists for any questions after receiving results

Transparent Pricing: Exceptional Value for Peace of Mind

Service Regular Price Special Price Savings
PLCB4 Gene Auriculocondylar Syndrome Type 2 NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Test Details:

  • Turnaround Time: 3-4 weeks
  • Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
  • Included Services: Genetic counselling session and family pedigree analysis
  • Technology: Next Generation Sequencing (NGS) for maximum accuracy

Why South African Families Trust Oracle Genomics

We’ve built our reputation on reliability and compassionate care:

  • Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Specialised in pediatric genetic conditions with experienced genetic counsellors
  • Advanced Technology: State-of-the-art NGS technology ensuring 99.9% accuracy
  • Patient-Centred Approach: We understand the emotional aspects of genetic testing and provide supportive care
  • Proven Track Record: Trusted by healthcare professionals and families nationwide

Take the First Step Toward Clarity Today

Don’t let uncertainty about genetic conditions continue to cause worry. Our PLCB4 Gene test provides the definitive answers you need to move forward with confidence.

Limited Time Special: Save ZAR 2,650 on this comprehensive genetic test. This special pricing won’t last forever.



Convenient Nationwide Access: With collection points across South Africa, getting tested is simple and stress-free. Contact us today to schedule your test and begin your journey to genetic clarity.