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ECE1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test

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

-28%

If you’re concerned about congenital central hypoventilation syndrome (CCHS) in your child or family, our ECE1 Gene DNA test provides the answers you need. This comprehensive NGS genetic test detects mutations in the ECE1 gene that can cause life-threatening breathing disorders in infants and children. 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 a history of unexplained breathing difficulties or sudden infant death. With nationwide coverage across South Africa including Johannesburg, Cape Town, Durban and Pretoria, we make genetic testing accessible and trustworthy. Early detection through this test can guide proper medical management and potentially save lives. Trust Oracle Genomics for professional genetic counselling and precise DNA analysis 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
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ECE1 Gene CHS DNA Test | ZAR 6
ECE1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Protect Your Child’s Breathing with ECE1 Gene Testing

As a parent, nothing matters more than your child’s health and safety. When breathing becomes a concern, the uncertainty can be overwhelming. Our ECE1 Gene Central Hypoventilation Syndrome DNA test provides the clarity and peace of mind you deserve. This advanced genetic screening helps identify congenital breathing disorders early, allowing for proper medical intervention and potentially life-saving management strategies.

Understanding the ECE1 Gene Test

The ECE1 gene plays a crucial role in regulating breathing during sleep. When mutations occur in this gene, it can lead to Congenital Central Hypoventilation Syndrome (CCHS) – a serious condition where the brain doesn’t properly control breathing, especially during sleep. Our Next-Generation Sequencing (NGS) technology examines your DNA with exceptional accuracy to detect these mutations, providing definitive answers about your genetic risk.

This isn’t just another test – it’s a comprehensive genetic analysis that examines the entire ECE1 gene sequence, ensuring no potential mutation goes undetected. Our advanced NGS methodology provides results you can trust for making informed healthcare decisions.

Who Should Consider This Test?

This test is particularly important if your child or family member experiences:

  • Unexplained breathing difficulties during sleep
  • History of sudden infant breathing pauses
  • Family history of CCHS or similar breathing disorders
  • Unexplained blueish skin colour (cyanosis) during sleep
  • Difficulty waking from sleep or excessive daytime sleepiness
  • Previous unexplained infant deaths in the family

If you’re planning a pregnancy and have family history of breathing disorders, this test can provide valuable pre-conception genetic information.

Why Early Detection Matters for Your Family’s Health

Early identification of ECE1 gene mutations can be life-changing. With proper diagnosis:

  • Your child can receive appropriate respiratory support during sleep
  • Medical teams can develop personalised monitoring and treatment plans
  • You gain peace of mind knowing the exact cause of breathing concerns
  • Family members can be screened for carrier status
  • Future pregnancies can be managed with genetic counselling support
  • Emergency situations can be prevented through proper preparation

Knowledge is power when it comes to managing congenital breathing disorders. This test provides that knowledge with clinical-grade accuracy.

Understanding Your Results – Clear Guidance Every Step

We understand that genetic test results can be confusing and anxiety-provoking. That’s why we provide:

  • Clear, easy-to-understand reports with plain language explanations
  • Professional genetic counselling included with your test to help interpret results
  • Family pedigree analysis to understand inheritance patterns
  • Direct connection to specialists who understand CCHS management
  • Ongoing support for any questions about your results

Whether your results show a mutation or provide reassuring negative findings, you’ll have the professional guidance needed to understand what it means for your family’s health.

Affordable Genetic Testing with Exceptional Value

Test Feature Details Value
Regular Price ZAR 9,350 Comprehensive genetic analysis
Special Price ZAR 6,700 Limited time savings of ZAR 2,650
Turnaround Time 3-4 Weeks Fast results for timely decisions
Sample Type Blood, Extracted DNA, or Blood on FTA Card Convenient collection options
Included Services Genetic Counselling + Family Pedigree Analysis ZAR 1,500+ value included

Considering the potential healthcare costs of undiagnosed breathing disorders, this test represents exceptional value for your family’s long-term health and peace of mind.

Why Trust Oracle Genomics?

We’ve built our reputation on accuracy, empathy, and professional excellence:

  • Nationwide Coverage – Testing available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise – Specialised in pediatric genetic conditions with years of experience
  • Advanced Technology – State-of-the-art NGS methodology for unparalleled accuracy
  • Patient-First Approach – We understand the emotional journey of genetic testing
  • Complete Confidentiality – Your genetic information is protected with the highest security standards
  • Insurance Guidance – Assistance with medical aid claims and reimbursement processes

Take the First Step Toward Answers Today

Don’t let uncertainty about your child’s breathing keep you awake at night. Our ECE1 Gene test provides the clarity you need to make informed healthcare decisions.

Multiple Ways to Book Your Test:

  • Online Booking – Secure 24/7 appointment scheduling
  • Telephone Consultation – Speak directly with our genetic counsellors
  • Clinic Visit – Personalised service at our nationwide locations
  • Home Collection – Convenient sample collection at your location (selected areas)

Limited Time Offer: Book now to secure your special price of ZAR 6,700 before this offer ends. Early detection could make all the difference for your child’s health and wellbeing.

Every day without answers is another day of uncertainty. Take control of your family’s genetic health today with confidence and professional support from Oracle Genomics.

Prefer to speak with someone? Call our genetic counselling team at [Phone Number] for personalised guidance