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ATP1A3 Gene Alternating Hemiplegia of Childhood Type 2 NGS Genetic DNA Test

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

-28%

Facing concerns about your child’s neurological health? Our ATP1A3 Gene Alternating Hemiplegia of Childhood Type 2 NGS Genetic DNA Test provides the answers you need for peace of mind. At only ZAR 6,700 (regularly ZAR 9,350), this comprehensive test uses advanced NGS technology to detect genetic mutations that cause this rare neurological disorder. We understand the anxiety parents feel when their child experiences unexplained symptoms, and our test delivers the clarity needed for proper diagnosis and treatment planning. With results in just 3-4 weeks and genetic counselling included, you’ll have the information to make informed healthcare decisions. Available nationwide across South Africa, including Johannesburg, Cape Town, and Durban, our test is backed by neurological specialists and cutting-edge technology. Take the first step toward understanding your child’s health with confidence and accuracy.

📞 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

ATP1A3 Gene AHC2 Test | ZAR 6
ATP1A3 Gene Alternating Hemiplegia of Childhood Type 2 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Your Child’s Neurological Health Starts Here

As a parent, watching your child experience unexplained neurological symptoms can be frightening and overwhelming. The ATP1A3 Gene Alternating Hemiplegia of Childhood Type 2 NGS Genetic DNA Test provides the clarity and answers you need to navigate this challenging journey with confidence.

What This Test Detects

This advanced genetic test specifically examines the ATP1A3 gene for mutations that cause Alternating Hemiplegia of Childhood Type 2 (AHC2). Using Next-Generation Sequencing (NGS) technology, we can identify even the smallest genetic variations that might be missed by conventional testing methods. This isn’t just a test – it’s a comprehensive genetic investigation that provides definitive answers about your child’s neurological condition.

Who Should Consider This Test

This test is essential for children experiencing:

  • Recurrent episodes of paralysis affecting different sides of the body
  • Unexplained seizures or movement disorders
  • Developmental delays with neurological symptoms
  • Family history of similar neurological conditions
  • Episodes triggered by stress, excitement, or temperature changes

If your child has been experiencing these symptoms without clear diagnosis, this test could provide the breakthrough answers you’ve been seeking.

Why Early Detection Matters for Your Child’s Future

Getting an accurate diagnosis through genetic testing can transform your child’s healthcare journey. Early identification of ATP1A3 mutations enables:

  • Personalised Treatment Plans: Tailored interventions based on your child’s specific genetic profile
  • Family Planning Guidance: Understanding inheritance patterns for future family decisions
  • Reduced Diagnostic Uncertainty: Ending the cycle of multiple doctor visits and inconclusive tests
  • Improved Quality of Life: Early intervention strategies to manage symptoms effectively
  • Peace of Mind: Knowing exactly what you’re dealing with reduces anxiety and uncertainty

Understanding Your Results with Compassion

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

  • Clear, Easy-to-Understand Reports: Written in plain language with medical terminology explained
  • Genetic Counselling Support: Professional guidance to help you understand the implications
  • Next Steps Guidance: Clear recommendations for follow-up care and specialist referrals
  • Ongoing Support: Access to our team for any questions after you receive your results

Whether the results confirm a diagnosis or rule out concerns, you’ll have the information needed to move forward with confidence.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
ATP1A3 Gene AHC2 NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

What’s Included: Comprehensive genetic analysis, genetic counselling session, detailed results report, and ongoing support.

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: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Neurological Specialists: Tests supervised by qualified neurologists and genetic specialists
  • Advanced NGS Technology: Cutting-edge genetic sequencing for maximum accuracy
  • Genetic Counselling Included: Professional support to help you understand your results
  • Proven Accuracy: Reliable results you can trust for critical healthcare decisions

Take the First Step Toward Answers Today

Don’t let uncertainty about your child’s neurological health continue. Every day without answers is another day of worry. Our ATP1A3 genetic test provides the clarity you need to move forward with confidence.

Limited Time Special: Save ZAR 2,650 on this comprehensive neurological genetic test

Fast Results: Get answers in just 3-4 weeks instead of months of uncertainty

Convenient Nationwide Access: Available across South Africa with easy sample collection

Book Your Test Today – Multiple Easy Options:

  • Online Booking: Secure online appointment scheduling available 24/7
  • Phone Consultation: Speak directly with our genetic counselling team
  • Clinic Visit: Visit our partner clinics in major cities nationwide
  • Home Collection: Convenient sample collection at your location

Your child’s neurological health deserves answers. Book your ATP1A3 genetic test today and take control of your family’s health journey with confidence and clarity.