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SCN2A Gene Dravet Syndrome NGS Genetic DNA Test

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

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Facing concerns about seizure disorders in your family? The SCN2A Gene Dravet Syndrome NGS Genetic DNA Test provides crucial answers for South African families. For only ZAR 6,700, this advanced genetic test uses Next Generation Sequencing technology to detect mutations in the SCN2A gene, which is responsible for severe epilepsy conditions. Early detection can significantly improve treatment outcomes and help manage seizure episodes more effectively. Our test offers peace of mind through accurate, reliable results processed by experienced neurologists. With nationwide coverage including Johannesburg, Cape Town, and Durban, we make genetic testing accessible across South Africa. Trust Oracle Genomics to provide the clarity your family needs to make informed healthcare decisions.

📞 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

SCN2A Dravet Syndrome DNA Test | ZAR 6
SCN2A Gene Dravet Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity for Seizure Disorders with SCN2A Dravet Syndrome Genetic Testing

When your child experiences unexplained seizures or you have a family history of epilepsy disorders, the uncertainty can be overwhelming. The SCN2A Gene Dravet Syndrome NGS Genetic DNA Test provides the answers South African families need to understand and manage these complex neurological conditions. At Oracle Genomics, we understand the emotional journey you’re facing and provide compassionate, accurate genetic testing to guide your family’s healthcare decisions.

Understanding the SCN2A Dravet Syndrome Test

The SCN2A gene plays a critical role in brain function, specifically in controlling sodium channels that regulate electrical activity in nerve cells. When mutations occur in this gene, it can lead to Dravet syndrome – a severe form of epilepsy that typically begins in infancy. Our advanced Next Generation Sequencing (NGS) technology examines your DNA with exceptional precision to identify these mutations, providing crucial information for diagnosis and treatment planning.

This isn’t just a test – it’s a pathway to understanding your child’s neurological health and creating an effective management strategy for seizure disorders.

Who Should Consider This Genetic Test?

This test is particularly important for families experiencing:

  • Infants or children with frequent, prolonged seizures
  • Family history of epilepsy or seizure disorders
  • Children whose seizures don’t respond well to standard medications
  • Developmental delays or regression following seizure onset
  • Unexplained febrile seizures in early childhood
  • Suspected genetic epilepsy syndromes

If you’re in Johannesburg, Cape Town, Durban, or anywhere in South Africa and recognize these symptoms in your child, this test could provide the diagnostic clarity needed for proper treatment.

Why Early Detection Matters for Your Child’s Health

Early identification of SCN2A mutations through genetic testing offers significant benefits:

  • Personalized Treatment: Knowing the specific genetic cause allows neurologists to tailor medication and therapy specifically for your child’s condition
  • Improved Seizure Management: Early intervention can help reduce the frequency and severity of seizures
  • Developmental Support: Understanding the genetic basis enables better educational and developmental planning
  • Family Planning Guidance: Provides valuable information for future family planning decisions
  • Peace of Mind: Reduces diagnostic uncertainty and empowers families with knowledge

Understanding Your Test Results

We know waiting for genetic test results can be anxiety-provoking. At Oracle Genomics, we provide clear, comprehensive result explanations that your neurologist can use to develop an effective treatment plan. Our genetic counselling support helps you understand what the results mean for your child’s health and your family’s future.

Your results will clearly indicate whether SCN2A gene mutations were detected and provide detailed information about what this means for seizure management and treatment options.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price
SCN2A Dravet Syndrome NGS Genetic Test ZAR 9,350 ZAR 6,700
Genetic Counselling Session Included
Family Pedigree Analysis Included
Results Interpretation Included

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

Considering the potential lifetime impact on your child’s health and development, this investment in genetic clarity provides exceptional long-term value.

Why Trust Oracle Genomics?

As South Africa’s trusted genetic testing provider, we offer:

  • Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Tests supervised by experienced neurologists and genetic specialists
  • Advanced Technology: State-of-the-art NGS technology for maximum accuracy
  • Comprehensive Support: Genetic counselling and family history analysis included
  • Patient-Centred Care: Empathetic support throughout your testing journey

Take the First Step Toward Clarity Today

Don’t let uncertainty about seizure disorders continue to worry your family. Early detection through genetic testing can make a significant difference in your child’s quality of life and treatment outcomes.

Book your SCN2A Dravet Syndrome Genetic Test now for only ZAR 6,700 and gain the clarity your family deserves.

Our genetic counselling team is ready to support you through this important healthcare decision. Contact Oracle Genomics today to schedule your test and take control of your family’s neurological health.