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PEX16 Gene Zellweger Syndrome NGS Genetic DNA Test

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

-28%

Facing concerns about rare neurological conditions in your family? The PEX16 Gene Zellweger Syndrome NGS Genetic DNA Test provides crucial answers for South African families. For only ZAR 6,700 (regularly ZAR 9,350), this advanced genetic test uses Next Generation Sequencing technology to detect mutations in the PEX16 gene, which is responsible for Zellweger syndrome – a serious peroxisomal disorder affecting brain development and function. Our comprehensive testing process includes genetic counselling to understand your family history and create a detailed pedigree chart. With results available in just 3-4 weeks, you’ll gain the clarity needed to make informed healthcare decisions. Trust Oracle Genomics for accurate, reliable genetic testing available nationwide across South Africa, including Johannesburg, Cape Town, and Durban. Early detection can provide peace of mind and guide appropriate medical management strategies.

📞 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

PEX16 Zellweger Syndrome DNA Test | ZAR 6
PEX16 Gene Zellweger Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding PEX16 Gene Zellweger Syndrome: Your Path to Clarity

When you’re worried about rare neurological conditions affecting your family, the uncertainty can be overwhelming. At Oracle Genomics, we understand the emotional weight of genetic concerns, especially when they involve serious conditions like Zellweger syndrome. Our PEX16 Gene NGS Genetic DNA Test provides the answers South African families need to move forward with confidence and clarity.

What This Test Detects

The PEX16 Gene Zellweger Syndrome test uses advanced Next Generation Sequencing (NGS) technology to identify mutations in the PEX16 gene. This gene plays a critical role in peroxisome biogenesis – essential cellular structures that help break down toxic substances and produce important compounds. When the PEX16 gene isn’t functioning properly, it can lead to Zellweger syndrome, a serious condition affecting brain development, liver function, and overall growth.

Our test provides comprehensive analysis of the PEX16 gene, giving you and your healthcare provider the detailed information needed to understand your genetic risk profile.

Who Should Consider This Test?

This test is particularly important for South African families experiencing:

  • Infants or children with developmental delays and neurological symptoms
  • Family history of Zellweger syndrome or related peroxisomal disorders
  • Unexplained liver dysfunction in young children
  • Vision or hearing problems in infancy
  • Muscle weakness or seizures in early childhood
  • Previous children with similar neurological concerns

If you’re planning a family and have concerns about genetic conditions, this test can provide valuable insights for future family planning decisions.

Why Early Detection Matters for Your Family’s Health

Getting answers through genetic testing can transform your family’s healthcare journey:

  • Peace of Mind: Eliminate uncertainty and gain clarity about genetic risks
  • Informed Decisions: Make better healthcare choices with accurate genetic information
  • Early Intervention: Access appropriate medical care and management strategies sooner
  • Family Planning: Understand risks for future pregnancies and make informed decisions
  • Reduced Anxiety: Replace worry with knowledge and a clear path forward

Early detection of PEX16 gene mutations can help guide treatment approaches and connect you with specialist care when needed.

Understanding Your Results

We know waiting for genetic test results can be stressful. At Oracle Genomics, we provide clear, comprehensive reports that your healthcare provider can easily interpret. Our genetic counselling support ensures you understand what your results mean for your family’s health.

Your results will clearly indicate whether PEX16 gene mutations were detected and what this means in terms of Zellweger syndrome risk. Our team is here to support you through every step of understanding your genetic information.

Transparent Pricing – Exceptional Value

Test Option Regular Price Special Price Savings
PEX16 Gene Zellweger Syndrome NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Preparation: Clinical history and genetic counselling session included

Considering the potential impact on your family’s health and future, this investment in genetic clarity provides exceptional long-term value.

Why Trust Oracle Genomics?

As South Africa’s leading genetic testing provider, we’re committed to your health and peace of mind:

  • Nationwide Coverage: Accessible testing across South Africa, including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Specialist neurologist oversight and genetic counselling support
  • Advanced Technology: Next Generation Sequencing for maximum accuracy
  • Patient-Focused Care: Empathetic support throughout your testing journey
  • Proven Reliability: Trusted by healthcare providers across South Africa

Take the First Step Toward Genetic Clarity Today

Don’t let uncertainty about genetic risks overshadow your family’s future. With our special pricing of ZAR 6,700, now is the perfect time to get the answers you need.

Book Your Test Today:
– Call our genetic counselling team for personalised guidance
– Schedule your sample collection at a convenient location near you
– Begin your journey to genetic clarity and peace of mind

Early detection through genetic testing can make all the difference in managing health concerns and planning for your family’s future. Contact Oracle Genomics today and take control of your genetic health journey.