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ST3GAL5 Gene Amish Infantile Epilepsy Syndrome NGS Genetic DNA Test

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

-28%

As a parent concerned about your child’s neurological health, our ST3GAL5 Gene Amish infantile epilepsy syndrome NGS Genetic DNA Test provides the clarity and peace of mind you deserve. This advanced genetic screening uses Next-Generation Sequencing technology to detect mutations in the ST3GAL5 gene, which is associated with severe infantile epilepsy syndromes. For only ZAR 6,700 (regularly ZAR 9,350), you gain access to precise diagnostic information that can guide treatment decisions and provide early intervention opportunities. Our test is particularly valuable for families with a history of infantile seizures or developmental delays. With results delivered within 3-4 weeks, you’ll receive comprehensive genetic counselling to help you understand your results and make informed healthcare decisions. Trust Oracle Genomics for accurate, reliable genetic testing that puts your family’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
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ST3GAL5 Epilepsy DNA Test | ZAR 6
ST3GAL5 Gene Amish Infantile Epilepsy 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 Your Child’s Neurological Health

As a parent, nothing matters more than your child’s wellbeing. When faced with concerns about seizures, developmental delays, or a family history of epilepsy, the uncertainty can be overwhelming. Our ST3GAL5 Gene Amish infantile epilepsy syndrome NGS Genetic DNA Test provides the answers you need to make confident healthcare decisions for your little one.

Understanding the ST3GAL5 Genetic Test

This advanced genetic screening examines the ST3GAL5 gene using Next-Generation Sequencing (NGS) technology, the gold standard in genetic testing. The ST3GAL5 gene plays a crucial role in brain development and function, and mutations in this gene are associated with severe forms of infantile epilepsy that typically appear in the first months of life.

Unlike traditional testing methods, our NGS approach provides comprehensive analysis of the entire gene, ensuring no potential mutations are missed. This thorough examination gives you and your healthcare provider the complete picture needed for accurate diagnosis and treatment planning.

Who Should Consider This Genetic Test?

This test is particularly important for:

  • Infants experiencing unexplained seizures or convulsions
  • Children with developmental delays or regression
  • Families with a history of infantile epilepsy syndromes
  • Parents concerned about genetic conditions affecting brain development
  • Healthcare providers seeking definitive diagnosis for complex neurological symptoms

If your child shows symptoms like muscle stiffness, feeding difficulties, or unusual eye movements in their first year, this test could provide critical diagnostic information.

Why Early Detection Matters for Your Child’s Future

Early diagnosis of ST3GAL5-related disorders can significantly impact your child’s quality of life and treatment outcomes. Benefits include:

  • Targeted Treatment Plans: Accurate diagnosis enables neurologists to develop specific treatment strategies
  • Early Intervention: Prompt identification allows for immediate therapeutic interventions
  • Family Planning Guidance: Understand inheritance patterns for future family planning
  • Reduced Diagnostic Uncertainty: End the cycle of multiple tests and uncertain diagnoses
  • Peace of Mind: Knowing the exact cause empowers you to make informed decisions

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. That’s why we provide comprehensive genetic counselling both before and after testing. Your results will clearly indicate:

  • Presence or absence of ST3GAL5 gene mutations
  • Specific genetic variations identified
  • Clinical significance of any findings
  • Recommended next steps and specialist referrals

Our genetic counsellors will walk you through every aspect of your results, ensuring you fully understand what they mean for your child’s health and your family’s future.

Transparent Pricing – Exceptional Value

Test Option Regular Price Special Price Savings
ST3GAL5 Gene NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

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

Consider this investment in your child’s health: early diagnosis can prevent years of uncertainty, multiple specialist visits, and potentially reduce long-term healthcare costs.

Why South African Families Trust Oracle Genomics

Nationwide Coverage: We serve families across South Africa with convenient testing locations in Johannesburg, Cape Town, Durban, and Pretoria.

Expert Genetic Counselling: Every test includes professional genetic counselling to help you understand your family’s genetic health.

Advanced Technology: We use state-of-the-art NGS technology for the most accurate results available.

Neurology Specialists: Our tests are developed in consultation with leading neurologists to ensure clinical relevance.

Comprehensive Preparation: We guide you through clinical history documentation and pedigree chart creation for complete family analysis.

Take the First Step Toward Clarity Today

Don’t let uncertainty about your child’s neurological health create unnecessary stress. Early detection through genetic testing can provide the answers you need to move forward with confidence.

Book Your Test Now: Contact us today to schedule your genetic counselling session and testing. Our compassionate team is ready to support you through every step of this important journey.

Limited time special pricing available – secure your family’s peace of mind while saving ZAR 2,650