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GABRG2 Gene Epilepsy Childhood Absence Type 2 NGS Genetic DNA Test

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

-28%

If your child experiences brief staring spells or sudden lapses in awareness, our GABRG2 Gene Epilepsy Test provides definitive answers. This comprehensive NGS genetic analysis specifically detects mutations linked to childhood absence epilepsy type 2, offering South African families clarity and direction. For only ZAR 6,700 (regularly ZAR 9,350), you’ll receive precise results within 3-4 weeks, accompanied by professional genetic counselling to understand your family’s inheritance patterns. Our trusted testing methodology gives you the confidence to make informed decisions about your child’s neurological care. Early detection can significantly improve treatment outcomes and quality of life. With nationwide coverage including Johannesburg, Cape Town, and Durban, accessing this life-changing information has never been more convenient.

📞 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

GABRG2 Epilepsy DNA Test | ZAR 6
GABRG2 Gene Epilepsy Childhood Absence Type 2 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Answers for Your Child’s Unexplained Staring Spells

When your child suddenly stops responding, stares blankly into space, or experiences brief lapses in awareness, it can be frightening and confusing. These moments might last just seconds, but the worry they create can feel endless. Our GABRG2 Gene Epilepsy Test provides the clarity South African families need to understand childhood absence seizures and take control of their child’s neurological health.

Understanding the GABRG2 Epilepsy Genetic Test

This advanced Next-Generation Sequencing (NGS) test specifically examines the GABRG2 gene, which plays a crucial role in brain function. When this gene contains mutations, it can disrupt normal brain activity and lead to childhood absence epilepsy type 2. Unlike general neurological assessments, our test provides definitive genetic evidence, giving you and your healthcare team concrete information to guide treatment decisions.

The testing process is straightforward and minimally invasive, requiring only a small blood sample or a single drop of blood on an FTA card. Our comprehensive approach includes genetic counselling to map your family’s health history, ensuring we understand the complete picture of your child’s genetic inheritance.

Is This Test Right for Your Child?

Consider this test if your child experiences:

  • Brief staring spells lasting 10-30 seconds
  • Sudden cessation of activity without falling
  • Repetitive blinking or slight mouth movements during episodes
  • Quick return to normal activity with no memory of the event
  • Multiple episodes occurring daily
  • Family history of epilepsy or similar neurological conditions

These symptoms often begin between ages 4-8 and may be mistaken for daydreaming or attention issues. Early genetic identification can prevent years of uncertainty and ensure appropriate treatment begins promptly.

Why Genetic Testing Matters for Your Child’s Future

Receiving a definitive genetic diagnosis provides numerous benefits for your family:

  • Targeted Treatment: Specific genetic information helps neurologists prescribe the most effective medications
  • Family Planning: Understand inheritance patterns for future family decisions
  • Educational Support: Schools can provide appropriate accommodations once the condition is medically confirmed
  • Peace of Mind: Replace uncertainty with clear understanding and a management plan
  • Early Intervention: Prevent potential learning difficulties or social challenges

Understanding Your Results with Compassion

Our team provides comprehensive result interpretation that focuses on empowerment rather than fear. Whether the test identifies a GABRG2 mutation or returns normal results, you’ll receive:

  • Clear, understandable explanation of findings
  • Discussion of what results mean for your child’s daily life
  • Guidance on next steps and available treatments
  • Connection to neurological specialists if needed
  • Ongoing support for questions or concerns

Remember: A genetic diagnosis doesn’t define your child – it provides the roadmap to help them thrive.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
GABRG2 Gene Epilepsy Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Genetic Counselling Session INCLUDED
Family Pedigree Analysis INCLUDED
Result Interpretation INCLUDED

Turnaround time: 3-4 weeks | Sample: Blood or DNA extract

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
  • Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
  • Advanced Technology: State-of-the-art NGS methodology ensuring 99.9% accuracy
  • Comprehensive Support: From initial consultation through result explanation
  • Proven Track Record: Thousands of South African families served with compassion and professionalism

Take the First Step Toward Clarity Today

Don’t let uncertainty about your child’s health continue. Every day without answers is a day without the right support and treatment. Our genetic counsellors are ready to help you understand if this test is appropriate for your family’s situation.

Multiple Ways to Begin Your Journey:

  • Online Booking: Schedule your consultation instantly
  • Telephone Assessment: Speak directly with our genetic specialists
  • Clinic Visit: Personal consultation at our nationwide locations

Limited Time Offer: The special price of ZAR 6,700 represents significant savings on this life-changing genetic analysis. Don’t miss this opportunity to gain the clarity your family deserves.

Early genetic identification can significantly improve treatment outcomes and prevent years of academic and social challenges. The window for optimal intervention is now – take action today.