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KCNQ2 Gene Early Infantile Epileptic Encephalopathy Type 7 NGS Genetic DNA Test

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

-28%

Facing concerns about your infant’s seizures or developmental delays? Our KCNQ2 gene test provides definitive answers for early infantile epileptic encephalopathy type 7. At ZAR 6,700 (regularly ZAR 9,350), this comprehensive NGS genetic test delivers accurate results within 3-4 weeks, giving you the clarity needed for proper treatment planning. We understand how overwhelming infant epilepsy can be, which is why our test includes genetic counselling to help you understand your family’s risk factors. With nationwide coverage across South Africa, including Johannesburg, Cape Town, and Durban, you can trust Oracle Genomics for reliable, professional genetic testing that puts your child’s health 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

KCNQ2 Epilepsy DNA Test ZAR 6
KCNQ2 Gene Early Infantile Epileptic Encephalopathy Type 7 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Finding Answers for Your Infant’s Epilepsy Journey

When your baby experiences seizures or developmental challenges, every moment counts. The uncertainty can be overwhelming, but you’re not alone. Our KCNQ2 gene test provides the clarity you need to understand early infantile epileptic encephalopathy type 7, giving you the power to make informed decisions about your child’s care.

Understanding the KCNQ2 Gene Test

This advanced genetic test examines the KCNQ2 gene using Next-Generation Sequencing (NGS) technology, the gold standard in genetic analysis. The KCNQ2 gene plays a crucial role in brain development and function, and mutations in this gene can cause early infantile epileptic encephalopathy type 7 – a rare but serious form of epilepsy that begins in the first months of life.

Our test doesn’t just provide a yes/no answer; it gives you comprehensive information about the specific genetic changes, helping your medical team develop the most effective treatment strategy for your child.

Who Should Consider This Test?

This test is particularly important if your infant shows:

  • Seizures beginning in the first 3 months of life
  • Developmental delays or regression
  • Abnormal EEG patterns
  • Family history of infantile epilepsy
  • Unexplained neurological symptoms
  • Resistance to standard anti-epileptic medications

Early diagnosis can significantly impact treatment outcomes and quality of life. Many parents find relief in having a definitive answer that guides their child’s medical care.

Why This Test Matters for Your Child’s Health

Getting the right diagnosis early can transform your child’s treatment journey. Benefits include:

  • Targeted Treatment: Specific genetic diagnoses can guide medication choices that work better for KCNQ2-related epilepsy
  • Family Planning: Understand inheritance patterns for future family planning decisions
  • Early Intervention: Begin appropriate therapies and interventions sooner
  • Peace of Mind: Replace uncertainty with knowledge and a clear path forward
  • Medical Guidance: Help your neurologist create the most effective care plan

Understanding Your Results

We know waiting for genetic test results can be anxiety-provoking. Our comprehensive report includes:

  • Clear explanation of genetic findings in understandable language
  • Detailed interpretation by our expert geneticists
  • Information about what the results mean for your child’s treatment
  • Guidance on next steps and additional testing if needed
  • Support resources for families facing similar challenges

Our genetic counselling session helps you understand the results and their implications for your entire family.

Transparent Pricing – Investing in Your Child’s Health

Service Regular Price Special Price
KCNQ2 Gene Test ZAR 9,350 ZAR 6,700
Genetic Counselling Included
Results Interpretation Included
Turnaround Time 3-4 Weeks

Consider this an investment in your child’s future – early, accurate diagnosis can prevent years of uncertainty and ineffective treatments.

Why Trust Oracle Genomics?

We understand the trust you place in us when seeking answers for your child’s health:

  • Nationwide Coverage: Accessible testing across South Africa, including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
  • Advanced Technology: State-of-the-art NGS technology for maximum accuracy
  • Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
  • Comprehensive Support: Includes genetic counselling and family pedigree analysis
  • Proven Track Record: Trusted by families and medical professionals nationwide

Take the First Step Toward Clarity

Don’t let uncertainty dictate your child’s health journey. Every day matters when it comes to early diagnosis and intervention.

Book your test today and get:

  • Definitive answers about your child’s condition
  • Personalised genetic counselling session
  • Clear, actionable results in 3-4 weeks
  • Peace of mind and a clear treatment path

Our team is ready to support you through this important journey. Contact us now to schedule your test and take control of your child’s health future.