Sale!

MECP2 Full Gene Mutation Analysis (RETT Syndrome)

Original price was: R6,700.Current price is: R5,000.

-25%

Facing concerns about developmental delays in your child? Our MECP2 Full Gene Mutation Analysis provides definitive answers about RETT Syndrome. For just ZAR 5,000 (regularly ZAR 6,700), this comprehensive test offers life-changing clarity for families across South Africa. Using advanced Sanger Sequencing technology, we deliver 99.9% accurate results within 8-10 days. Early detection means earlier intervention and better quality of life. Our compassionate team understands the emotional journey you’re on and provides clear, understandable results with expert guidance. Trust Oracle Genomics for reliable genetic testing that puts your family’s wellbeing 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

RETT Syndrome Genetic Testing ZAR 5
MECP2 Full Gene Mutation Analysis (RETT Syndrome)
R6,700 Original price was: R6,700.R5,000Current price is: R5,000.

[wpforms id=”1190″ title=”true” description=”Request a call back”]

Understanding RETT Syndrome: Your Path to Clarity and Peace of Mind

When your child shows signs of developmental regression or unusual hand movements, the uncertainty can be overwhelming. We understand the emotional rollercoaster you’re experiencing. Our MECP2 Full Gene Mutation Analysis provides the definitive answers you need to move forward with confidence and create the best possible care plan for your child.

What This Test Reveals About Your Child’s Health

The MECP2 gene plays a crucial role in brain development and function. When mutations occur in this gene, they can lead to RETT Syndrome – a rare genetic disorder that primarily affects girls. Our comprehensive analysis examines the entire MECP2 gene using gold-standard Sanger Sequencing technology, providing you with the most accurate genetic information available.

This isn’t just a test; it’s a roadmap to understanding your child’s unique needs and creating targeted interventions that can significantly improve their quality of life.

Is This Test Right for Your Child?

If your daughter is experiencing any of these symptoms, genetic testing could provide crucial answers:

  • Loss of purposeful hand skills between 6-18 months
  • Developmental regression or slowed development
  • Repetitive hand movements (hand-wringing, washing, clapping)
  • Problems with walking or coordination
  • Breathing difficulties while awake
  • Social withdrawal or communication challenges

Early diagnosis means earlier access to specialised therapies and support services that can make a profound difference in your child’s development.

Why Early Detection Matters for Your Family

Getting a definitive diagnosis through MECP2 testing provides multiple life-changing benefits:

  • Peace of Mind: End the uncertainty and move forward with confidence
  • Targeted Care: Access specialised therapies and interventions
  • Family Planning: Understand genetic risks for future pregnancies
  • Educational Support: Secure appropriate school accommodations
  • Community Connection: Connect with other RETT Syndrome families

Knowledge is power – and in this case, knowledge means better quality of life for your child and your entire family.

Understanding Your Results: Clear Guidance Every Step

We know genetic test results can feel overwhelming. That’s why we provide:

  • Plain Language Reports: No confusing medical jargon – just clear, understandable results
  • Expert Consultation: Access to genetic counsellors who explain what your results mean
  • Actionable Next Steps: Clear guidance on treatment options and support services
  • Ongoing Support: We’re here to answer questions even after you receive your results

Your results will clearly indicate whether an MECP2 mutation was detected and what that means for your child’s care plan.

Transparent Pricing – No Hidden Costs

Service Regular Price Special Price Savings
MECP2 Full Gene Mutation Analysis ZAR 6,700 ZAR 5,000 ZAR 1,700

Test Details:

  • Turnaround Time: 8-10 days
  • Sample Type: Peripheral blood
  • Method: Sanger Sequencing (gold standard)
  • Accuracy: 99.9% reliable results

This investment in your child’s health could save thousands in unnecessary treatments and provide clarity that’s truly priceless.

Why Thousands of South African Families Trust Oracle Genomics

Nationwide Coverage: Convenient testing locations in Johannesburg, Cape Town, Durban, Pretoria and across South Africa

Medical Expertise: Our tests are conducted by certified genetic specialists with years of experience

Accuracy Guarantee: We use only the most advanced, clinically validated testing methods

Patient-Centred Care: We understand the emotional journey and provide compassionate support throughout

Quick Results: Get answers in just 8-10 days, not weeks or months

Take the First Step Toward Clarity Today

Don’t let uncertainty about your child’s development continue to cause stress and worry. The answers you need are within reach.

Book Your Test Now: Call 0861 123 456 or visit our website to schedule your appointment

Convenient Locations: Testing available at multiple centres across major cities

Doctor’s Prescription: Required for this test – we can help coordinate if needed

Every day matters when it comes to your child’s development. Take action today and get the clarity your family deserves.