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SLC25A15 Gene Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome NGS Genetic DNA Test

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

-28%

If you’re concerned about unexplained neurological symptoms, developmental delays, or metabolic issues in your family, our SLC25A15 genetic test provides crucial answers. This comprehensive NGS DNA test detects Hyperornithinemia-Hyperammonemia-Homocitrullinuria syndrome, a rare but serious metabolic disorder that affects ammonia processing in the body. For only ZAR 6,700 (regularly ZAR 9,350), you’ll receive accurate results within 3-4 weeks, helping you understand your genetic risk and make informed health decisions. Our test includes professional genetic counselling to help interpret your family history and results, giving you the clarity and confidence you need. With nationwide coverage across South Africa including Johannesburg, Cape Town, and Durban, accessing this specialised testing has never been easier. Early detection can significantly improve management strategies and quality of life for affected individuals.

📞 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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SLC25A15 Genetic Test ZAR 6
SLC25A15 Gene Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity About Rare Metabolic Conditions with Our SLC25A15 Genetic Test

When unexplained neurological symptoms, developmental concerns, or metabolic issues affect your family, the uncertainty can be overwhelming. Our SLC25A15 genetic test provides the answers you need to understand and manage Hyperornithinemia-Hyperammonemia-Homocitrullinuria syndrome – a rare but serious metabolic disorder that impacts how your body processes ammonia.

Understanding Your SLC25A15 Genetic Test

This specialised Next-Generation Sequencing (NGS) test examines the SLC25A15 gene, which plays a critical role in your body’s ability to process ammonia. When this gene doesn’t function properly, it can lead to Hyperornithinemia-Hyperammonemia-Homocitrullinuria syndrome – a condition where ammonia builds up in the bloodstream, potentially causing neurological damage and other serious health complications.

Our test uses advanced NGS technology to provide comprehensive analysis of your genetic makeup, giving you and your healthcare provider the detailed information needed for accurate diagnosis and effective management strategies.

Who Should Consider This Genetic Test?

This test is particularly important if you or your family members experience:

  • Unexplained neurological symptoms or developmental delays
  • Recurrent episodes of confusion, lethargy, or coma
  • Family history of metabolic disorders
  • Elevated ammonia levels in blood tests
  • Feeding difficulties or failure to thrive in infants
  • Unexplained seizures or movement disorders
  • Developmental regression in children

Early detection through genetic testing can help prevent serious complications and guide appropriate treatment approaches.

Why Early Detection Matters for Your Health

Getting tested provides multiple important benefits:

  • Peace of Mind: Eliminate uncertainty about your genetic risk
  • Early Intervention: Begin appropriate management before serious complications develop
  • Family Planning: Understand inheritance patterns for future family decisions
  • Personalised Care: Work with your doctor to create targeted treatment plans
  • Prevent Complications: Reduce risk of neurological damage through proper management

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. That’s why we provide:

  • Clear, Easy-to-Understand Reports: Your results will be presented in straightforward language with clear explanations
  • Professional Support: Access to genetic counselling to help interpret your results
  • Medical Guidance: Results that your healthcare provider can use to develop appropriate care plans
  • Family Implications: Information about what your results mean for other family members

Remember: A positive result doesn’t necessarily mean you’ll develop symptoms, and our genetic counsellors will help you understand what your specific results mean for your health.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
SLC25A15 Genetic Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Your investment includes:

  • Comprehensive NGS genetic analysis
  • Professional genetic counselling session
  • Detailed results report with clinical interpretation
  • 3-4 week turnaround time
  • Nationwide coverage across South Africa

Why Trust Oracle Genomics?

We’ve built our reputation on accuracy, compassion, and professional excellence:

  • Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Advanced Technology: State-of-the-art NGS testing for maximum accuracy
  • Expert Team: Qualified genetic counsellors and medical professionals
  • Patient-Focused Care: We understand the emotional journey of genetic testing
  • Proven Accuracy: Reliable results you can trust for important health decisions

Take Control of Your Health Journey Today

Don’t let uncertainty about genetic risks control your life. Early detection through our SLC25A15 genetic test can provide the clarity and direction you need for better health outcomes.

Ready to get started? Contact us today to schedule your genetic counselling session and testing. Our team is here to support you every step of the way.

Multiple Ways to Book Your Test:

  • Online Booking: Schedule your appointment through our secure portal
  • Phone Consultation: Speak directly with our genetic counselling team
  • Clinic Visit: Visit one of our nationwide locations

Limited time special pricing available – secure your test at ZAR 6,700 before this offer ends!

Test Specifications:

  • Turnaround Time: 3-4 weeks
  • Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
  • Preparation Required: Clinical history and genetic counselling session
  • Testing Method: Next-Generation Sequencing (NGS) Technology
  • Specialty: General Physician / Metabolic Genetics