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KCNQ3 Gene Seizures Benign Neonatal Type 2 NGS Genetic DNA Test

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

-28%

If you’re concerned about benign neonatal seizures in your family, our KCNQ3 Gene Seizures NGS Genetic DNA Test provides the answers you need. For just ZAR 6,700, this comprehensive test uses advanced Next Generation Sequencing technology to detect mutations in the KCNQ3 gene that cause benign neonatal seizures type 2. Early detection can help manage symptoms effectively and provide peace of mind for South African families. Our test is conducted with the highest accuracy standards, and we offer genetic counselling to help you understand your family’s risk. With nationwide coverage including Johannesburg, Cape Town, and Durban, getting tested has never been more accessible. Take control of your family’s neurological health today with our trusted genetic testing service.

📞 24/7 South African Support Team Call : +27 6412 56421

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
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KCNQ3 Gene Seizures Test | ZAR 6
KCNQ3 Gene Seizures Benign Neonatal 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 Benign Neonatal Seizures with KCNQ3 Gene Testing

As a parent, nothing is more concerning than watching your newborn experience seizures. The uncertainty and worry can be overwhelming, but you don’t have to face these questions alone. Our KCNQ3 Gene Seizures Benign Neonatal Type 2 NGS Genetic DNA Test provides the clarity and answers South African families need to understand their child’s neurological health.

Understanding the KCNQ3 Gene Seizures Test

This specialised genetic test examines the KCNQ3 gene, which plays a crucial role in regulating electrical activity in the brain. When mutations occur in this gene, it can lead to benign neonatal seizures type 2 – a condition that typically appears in the first few days of life. Using advanced Next Generation Sequencing (NGS) technology, we can accurately identify these genetic variations, giving you definitive answers about your child’s condition.

The test is conducted under the supervision of experienced neurologists and includes genetic counselling to help you understand your family’s complete health picture.

Who Should Consider This Test?

This test is particularly important for:

  • Newborns experiencing seizures within the first week of life
  • Families with a history of benign neonatal seizures
  • Parents concerned about genetic neurological conditions
  • Infants showing seizure symptoms that resolve spontaneously
  • Families planning future pregnancies who want to understand genetic risks

If your baby has experienced brief seizure episodes, often described as ‘jittery’ movements or brief stiffness, this test can provide crucial diagnostic information.

Why Early Detection Matters for Your Family’s Health

Getting a definitive diagnosis through genetic testing offers multiple benefits:

  • Peace of Mind: Knowing the exact cause of seizures reduces uncertainty and anxiety
  • Proper Management: Understanding the genetic basis helps healthcare providers create appropriate care plans
  • Family Planning: Identifies inheritance patterns for future family planning decisions
  • Early Intervention: Allows for timely management strategies that can improve outcomes
  • Reduced Hospital Stays: Clear diagnosis can prevent unnecessary medical investigations

Many families find that understanding the genetic basis of their child’s condition brings tremendous relief and enables them to focus on appropriate care.

Understanding Your Test Results

Our genetic counselling team will walk you through your results with compassion and clarity:

  • Positive Result: If a KCNQ3 gene mutation is detected, our specialists will explain what this means for your child’s health and provide guidance on management options
  • Negative Result: If no mutation is found, this can help rule out benign neonatal seizures type 2 and guide further investigation
  • Genetic Counselling: Every test includes a session to help you understand the results and their implications for your family

Remember: A positive result doesn’t change who your child is – it provides valuable information to help them thrive.

Affordable Genetic Testing for South African Families

Test Feature Details Value
Regular Price ZAR 9,350 Comprehensive genetic analysis
Special Price ZAR 6,700 Limited time offer
Turnaround Time 3-4 Weeks Timely results for urgent decisions
Sample Type Blood, DNA, or FTA Card Convenient collection options

Considering the peace of mind and potential healthcare savings from accurate diagnosis, this test represents excellent value for South African families.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
  • Advanced Technology: State-of-the-art NGS technology for maximum accuracy
  • Genetic Counselling: Comprehensive support throughout your testing journey
  • Proven Track Record: Trusted by healthcare providers across South Africa

Take the First Step Toward Answers Today

Don’t let uncertainty about your child’s health create unnecessary stress. Our KCNQ3 Gene Seizures Test provides the clarity you need to make informed decisions about your family’s neurological health.

Book your test now while the special ZAR 6,700 pricing is available. Early detection can make a significant difference in management and peace of mind.

Multiple Booking Options Available:

  • Online booking through our secure portal
  • Telephone consultations with our genetic counsellors
  • Referrals from your healthcare provider
  • Walk-in appointments at our nationwide centres

Your family’s health journey deserves the clarity and confidence that comes from accurate genetic testing. Contact us today to schedule your KCNQ3 Gene Seizures Test.