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CHD7 Gene CHARGE Syndrome NGS Genetic DNA Test

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

-28%

Facing concerns about CHARGE syndrome in your family? Our CHD7 Gene CHARGE Syndrome NGS Genetic DNA Test provides the clarity and peace of mind you deserve. For just ZAR 6,700 (regularly ZAR 9,350), this advanced genetic test uses Next-Generation Sequencing technology to deliver highly accurate results within 3-4 weeks. We understand the emotional journey of genetic testing and provide compassionate support throughout the process. Our test helps identify mutations in the CHD7 gene, giving you the information needed to make informed healthcare decisions. With nationwide coverage across South Africa including Johannesburg, Cape Town, and Durban, we make professional genetic testing accessible to all families. Trust Oracle Genomics for reliable, confidential testing backed by medical expertise and genetic counselling support.

📞 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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CHD7 Gene CHARGE Syndrome DNA Test | ZAR 6
CHD7 Gene CHARGE Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding CHARGE Syndrome: Your Path to Genetic Clarity

When you’re concerned about your child’s development or have a family history of CHARGE syndrome, the uncertainty can feel overwhelming. We understand the emotional weight of genetic questions and the need for clear, reliable answers. Our CHD7 Gene CHARGE Syndrome NGS Genetic DNA Test provides the scientific certainty you need to move forward with confidence and make informed decisions about your family’s health journey.

What This Test Reveals About Your Genetic Health

The CHD7 Gene CHARGE Syndrome test examines the CHD7 gene using advanced Next-Generation Sequencing (NGS) technology. This sophisticated approach allows us to detect even the smallest genetic variations that could indicate CHARGE syndrome – a complex condition affecting multiple body systems including vision, hearing, heart function, and growth development.

Unlike basic genetic tests, our NGS technology provides comprehensive analysis of the entire CHD7 gene, ensuring no potential mutation goes undetected. This thorough approach gives you and your healthcare providers the complete picture needed for accurate diagnosis and proper management planning.

Is This Test Right for Your Family?

This test is particularly important if your child or family member shows signs that might indicate CHARGE syndrome, including:

  • Coloboma (eye abnormalities affecting vision)
  • Heart defects present from birth
  • Choanal atresia (nasal passage blockage)
  • Growth retardation or developmental delays
  • Ear abnormalities and hearing loss
  • Multiple congenital anomalies affecting different body systems

If you have a family history of CHARGE syndrome or related conditions, this test can provide crucial information for family planning and early intervention strategies.

Why Early Detection Matters for Your Child’s Future

Getting clear answers about CHARGE syndrome can transform your family’s healthcare journey. Early genetic confirmation enables:

  • Targeted Medical Care: Specific management plans for heart, hearing, vision, and developmental needs
  • Early Intervention: Access to specialised therapies and support services when they’re most effective
  • Family Planning Guidance: Understanding inheritance patterns for future family decisions
  • Reduced Diagnostic Uncertainty: Ending the stressful search for answers and beginning focused treatment
  • Peace of Mind: Knowing you have accurate information to guide your child’s healthcare journey

Understanding Your Results with Compassionate Support

We know that waiting for genetic test results can be an anxious time. That’s why we provide:

  • Clear, Understandable Reports: Your results come with plain-language explanations you can understand
  • Genetic Counselling Session: Included with your test to help interpret results and discuss implications
  • Family Pedigree Analysis: We map your family history to provide context for your results
  • Medical Referral Support: Guidance on next steps with appropriate healthcare specialists
  • Ongoing Support: Our team remains available to answer questions as you process your results

Whether your results confirm CHARGE syndrome or provide reassuring information, you’ll have the professional support needed to understand what they mean for your family.

Transparent Pricing – Exceptional Value for Peace of Mind

Service Regular Price Special Price Savings
CHD7 Gene CHARGE Syndrome NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Your investment includes: Comprehensive genetic analysis, genetic counselling session, family pedigree chart, detailed results report, and professional medical interpretation.

Turnaround Time: 3-4 weeks from sample receipt
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Tests conducted by qualified genetic specialists and paediatric consultants
  • Advanced Technology: State-of-the-art NGS technology for unparalleled accuracy
  • Confidential Service: Your privacy and genetic information are protected with strict confidentiality
  • Compassionate Care: We understand the emotional aspects of genetic testing and provide supportive guidance
  • Proven Reliability: Trusted by healthcare providers and families throughout South Africa

Take the First Step Toward Genetic Clarity Today

Don’t let uncertainty about CHARGE syndrome delay your family’s path to answers and appropriate care. Our special pricing of ZAR 6,700 makes professional genetic testing accessible when you need it most.

Ready to begin? Contact us today to schedule your genetic counselling session and testing. Our compassionate team will guide you through every step, from initial consultation to understanding your results.

Call now or book online to secure your testing appointment and take control of your family’s genetic health journey.

Preparing for Your Test

To ensure the most accurate results, please bring:

  • Complete clinical history of the patient
  • Information about family members affected by similar conditions
  • Any previous genetic test results or medical reports

Our genetic counselling session will help create a comprehensive family pedigree chart to support accurate analysis and interpretation of your results.