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STAMBP Gene Microcephaly-Capillary Malformation Syndrome NGS Genetic DNA Test

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

-28%

Facing concerns about microcephaly or unusual capillary malformations in your family? Our STAMBP Gene NGS Genetic DNA Test provides the answers you need for peace of mind. For just ZAR 6,700 (regularly ZAR 9,350), this comprehensive test uses advanced Next-Generation Sequencing technology to detect mutations associated with microcephaly-capillary malformation syndrome. Early detection can help guide appropriate medical care and management strategies. The test includes essential genetic counselling to help you understand your family’s risk patterns and make informed health decisions. With results available in 3-4 weeks and nationwide coverage across South Africa, including Johannesburg, Cape Town, and Durban, we make genetic testing accessible and reliable. Trust Oracle Genomics for accurate, compassionate genetic care 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
Guaranteed Safe Checkout

STAMBP Gene Test ZAR 6
STAMBP Gene Microcephaly-Capillary Malformation Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Your Family’s Genetic Health Journey

When you notice unusual capillary malformations or concerns about head size development in your child, the uncertainty can be overwhelming. At Oracle Genomics, we understand the emotional weight of these observations and provide the clarity you need through our specialised STAMBP Gene testing. Our compassionate approach combines cutting-edge science with personalised care to help South African families navigate complex genetic conditions with confidence.

What This Test Reveals About Your Health

The STAMBP Gene NGS Genetic DNA Test examines specific genetic markers associated with microcephaly-capillary malformation syndrome – a rare condition that affects brain development and blood vessel formation. Using Next-Generation Sequencing technology, we analyse the STAMBP gene for mutations that could impact your family’s health. This isn’t just a test; it’s a pathway to understanding and managing potential health challenges with precision and care.

When This Test Could Provide Answers

  • Your child has an unusually small head circumference (microcephaly)
  • Presence of distinctive capillary malformations or birthmarks
  • Family history of developmental delays or neurological concerns
  • Unexplained seizures or movement disorders in childhood
  • Multiple family members with similar physical characteristics
  • Planning for pregnancy with known family genetic history

If any of these situations resonate with your family’s experience, this test could provide the clarity needed for better health management.

Why Early Detection Matters for Your Family’s Future

Knowledge is power when it comes to genetic conditions. Early detection through our STAMBP Gene test enables:

  • Proactive Healthcare Planning: Work with specialists to develop targeted care strategies
  • Informed Family Decisions: Understand inheritance patterns for future family planning
  • Reduced Diagnostic Uncertainty: Move from suspicion to certainty with precise genetic answers
  • Access to Specialised Care: Connect with neurologists and genetic specialists who understand your specific needs
  • Peace of Mind: Replace anxiety with actionable information and support

Understanding Your Results with Compassion

We know that waiting for genetic test results can be stressful. That’s why we provide comprehensive support throughout the process. Your results will be clearly explained by our genetic counselling team, who will help you understand what the findings mean for your family’s health. Whether the results provide reassurance or identify areas needing attention, you’ll have a dedicated team to guide your next steps with empathy and expertise.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price
STAMBP Gene NGS Genetic DNA Test ZAR 9,350 ZAR 6,700
Genetic Counselling Session INCLUDED
Family Pedigree Analysis INCLUDED
Results Interpretation INCLUDED

Consider the long-term value: Early detection can prevent years of uncertainty and guide appropriate medical interventions that may save significantly on future healthcare costs.

Why South African Families Trust Oracle Genomics

  • Nationwide Accessibility: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
  • Advanced Technology: Using reliable NGS methodology for accurate results
  • Comprehensive Support: Genetic counselling included to ensure you understand your results
  • Proven Track Record: Trusted by healthcare professionals throughout South Africa

Take the First Step Toward Genetic Clarity Today

Don’t let uncertainty about your family’s genetic health create unnecessary stress. Our team is ready to provide the answers and support you need. With convenient testing locations across major South African cities and comprehensive genetic counselling included, there’s never been a better time to gain clarity.

Multiple Ways to Begin Your Health Journey:

  • Online Booking: Schedule your test and genetic counselling session in minutes
  • Telephone Consultation: Speak directly with our genetic specialists
  • Clinic Visit: Visit our facilities in Johannesburg, Cape Town, or Durban
  • Mobile Testing: We can arrange convenient sample collection

Limited Time Special Pricing: Secure your test at ZAR 6,700 before this offer ends. Your family’s health journey deserves the clarity and confidence that comes from professional genetic testing.

Ready for Answers? Contact Oracle Genomics today and take control of your family’s genetic health story. Early detection leads to better outcomes – don’t wait for certainty.

Test Specifications

  • Turnaround Time: 3 to 4 Weeks
  • Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card
  • Preparation Required: Clinical History and Genetic Counselling Session
  • Medical Specialty: Neurology
  • Testing Method: Next-Generation Sequencing (NGS) Technology