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CACNA1H Gene Epilepsy Childhood Absence Type 6 Susceptibility NGS Genetic DNA Test

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

-28%

If you’re concerned about childhood absence epilepsy in your family, our CACNA1H Gene Epilepsy Susceptibility Test provides crucial answers. This comprehensive NGS genetic DNA test specifically detects susceptibility to childhood absence type 6 epilepsy, offering families in South Africa the clarity they need. For only ZAR 6,700 (regularly ZAR 9,350), you’ll receive accurate results using advanced next-generation sequencing technology. Our test includes professional genetic counselling to create a detailed family pedigree chart, ensuring you understand your genetic risk factors. With results in 3-4 weeks and nationwide coverage including Johannesburg, Cape Town, and Durban, we make genetic testing accessible and trustworthy for South African families seeking answers about epilepsy susceptibility.

📞 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

CACNA1H Epilepsy Genetic Test ZAR 6
CACNA1H Gene Epilepsy Childhood Absence Type 6 Susceptibility 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 Epilepsy Risk: CACNA1H Gene Testing for South African Families

When your child experiences unexplained staring spells or brief lapses in awareness, it’s natural to feel concerned and seek answers. Childhood absence epilepsy can be subtle yet impactful, affecting your child’s daily life and development. Our CACNA1H Gene Epilepsy Susceptibility Test provides the clarity South African families need to understand genetic risk factors and make informed healthcare decisions.

What This Test Reveals About Childhood Absence Epilepsy

The CACNA1H gene plays a crucial role in calcium channel function in brain cells. When this gene has specific variations, it can increase susceptibility to childhood absence type 6 epilepsy – a form characterised by brief staring spells where children temporarily lose awareness of their surroundings. Our advanced NGS (Next-Generation Sequencing) technology examines this gene with exceptional accuracy, providing reliable results that help neurologists understand your child’s specific genetic profile.

Is This Test Right for Your Family?

Consider this genetic test if your child experiences:

  • Frequent staring spells lasting 10-20 seconds
  • Brief lapses in awareness or responsiveness
  • Repetitive movements like lip smacking or eye blinking during episodes
  • Family history of epilepsy or seizure disorders
  • Unexplained learning difficulties or attention problems

Early genetic understanding can help guide appropriate treatment and management strategies, potentially improving your child’s quality of life and educational outcomes.

Why Early Genetic Understanding Matters

Discovering your child’s genetic susceptibility to childhood absence epilepsy provides multiple benefits:

  • Personalised Treatment Plans: Results help neurologists tailor medication and management approaches
  • Reduced Diagnostic Uncertainty: Move from suspicion to certainty about genetic factors
  • Family Planning Insights: Understand inheritance patterns for future family planning
  • Early Intervention Opportunities: Implement strategies before symptoms significantly impact development
  • Peace of Mind: Replace anxiety with understanding and proactive management

Understanding Your Genetic Results

Our comprehensive reporting makes complex genetic information accessible and meaningful:

  • Clear Interpretation: Results explained in straightforward language you can understand
  • Genetic Counselling Session: Included professional guidance to discuss findings and implications
  • Family Pedigree Analysis: Visual mapping of how epilepsy may affect your family
  • Next Steps Guidance: Practical recommendations for working with your neurologist
  • Ongoing Support: Access to resources and information as your child grows

Remember: A positive result indicates susceptibility, not certainty – it’s valuable information for proactive healthcare.

Affordable Genetic Testing for South African Families

Service Regular Price Special Price Value
CACNA1H Gene Test ZAR 9,350 ZAR 6,700 28% Savings
Genetic Counselling INCLUDED
Family Pedigree Analysis INCLUDED
Results Interpretation INCLUDED

Turnaround time: 3-4 weeks | Sample: Blood, Extracted DNA, or FTA Card

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Accessible testing across 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 sequencing for maximum accuracy
  • Patient-Centred Care: Empathetic support throughout your testing journey
  • Proven Reliability: Trusted by healthcare professionals across South Africa

Take the First Step Toward Understanding

Don’t let uncertainty about childhood epilepsy risk create unnecessary anxiety. Our CACNA1H Gene Test provides the answers South African families need to move forward with confidence.

Limited Time Offer: Save ZAR 2,650 on comprehensive genetic testing including professional counselling

Convenient Sampling: Choose from blood draw, extracted DNA, or simple FTA card options

Nationwide Access: Available throughout South Africa with results delivered securely

Book Your Genetic Test Today

Online: Complete our secure booking form

Telephone: Speak directly with our genetic counselling team

Clinic Visit: Schedule at a partner facility near you

Your child’s neurological health deserves the clarity that modern genetic science can provide. Contact Oracle Genomics today and take control of your family’s health journey.