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MT-ND3 Gene Leigh Syndrome Mitochondrial Complex I Deficiency NGS Genetic DNA Test

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

-28%

Facing concerns about mitochondrial disorders or neurological symptoms in your family? Our MT-ND3 Gene Leigh Syndrome NGS Genetic DNA Test provides definitive answers and peace of mind. For only ZAR 6,700 (regularly ZAR 9,350), this comprehensive test uses advanced Next-Generation Sequencing technology to detect mutations in the MT-ND3 gene that cause mitochondrial complex I deficiency. Early detection can help manage symptoms, guide treatment decisions, and provide crucial information for family planning. Our expert genetic counselling session included with every test ensures you understand your results and their implications. With nationwide coverage across South Africa including Johannesburg, Cape Town, and Durban, we make advanced genetic testing accessible and trustworthy. Take control of your family’s health journey with confidence and clarity.

📞 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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MT-ND3 Leigh Syndrome Genetic Test | ZAR 6
MT-ND3 Gene Leigh Syndrome Mitochondrial Complex I Deficiency NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity and Peace of Mind with MT-ND3 Leigh Syndrome Genetic Testing

When neurological symptoms appear in your family, the uncertainty can be overwhelming. You deserve clear answers and a path forward. Our MT-ND3 Gene Leigh Syndrome NGS Genetic DNA Test provides the definitive diagnosis you need to make informed healthcare decisions for your loved ones.

Understanding Your MT-ND3 Genetic Test

This advanced genetic test specifically examines the MT-ND3 gene using Next-Generation Sequencing (NGS) technology. The MT-ND3 gene plays a crucial role in mitochondrial function – the energy powerhouses of your cells. When mutations occur in this gene, it can lead to Leigh syndrome, a severe neurological disorder that typically appears in infancy or early childhood.

Our test doesn’t just provide a yes/no answer. It gives you comprehensive information about the specific genetic variations present, helping your healthcare team develop the most appropriate management plan.

Who Should Consider This Genetic Test?

This test is particularly important if you or your child experience:

  • Progressive neurological deterioration in infancy or childhood
  • Developmental regression or delayed milestones
  • Muscle weakness, poor muscle tone, or movement disorders
  • Breathing difficulties or respiratory problems
  • Feeding difficulties and failure to thrive
  • Family history of mitochondrial disorders or Leigh syndrome
  • Unexplained neurological symptoms in multiple family members

Early testing can provide crucial information for managing symptoms and planning appropriate care.

Why Early Detection Matters for Your Family’s Health

Getting a definitive diagnosis through genetic testing offers multiple life-changing benefits:

  • Accurate Diagnosis: Move from uncertainty to clarity with a precise genetic confirmation
  • Personalised Treatment: Guide your medical team in developing targeted management strategies
  • Family Planning Insights: Understand inheritance patterns for future family decisions
  • Reduced Diagnostic Odyssey: Avoid years of unnecessary tests and medical appointments
  • Peace of Mind: Replace anxiety with knowledge and a clear path forward
  • Early Intervention: Implement supportive therapies at the earliest possible stage

Understanding Your Test Results with Confidence

We understand that waiting for genetic test results can be anxiety-provoking. That’s why we include expert genetic counselling with every test. Your genetic counsellor will:

  • Explain your results in clear, understandable language
  • Discuss what the findings mean for your health and your family
  • Help you understand inheritance patterns and risks
  • Connect you with appropriate resources and support networks
  • Guide discussions with your healthcare providers

With results typically available within 3-4 weeks, you won’t face prolonged uncertainty.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
MT-ND3 Leigh Syndrome NGS Genetic Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Genetic Counselling Session INCLUDED at no extra cost
Family Pedigree Analysis INCLUDED with every test

This comprehensive package represents exceptional value, providing not just testing but complete support throughout your genetic health journey.

Why Trust Oracle Genomics?

We’ve built our reputation on accuracy, empathy, and accessibility:

  • 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
  • Patient-First Approach: Every test includes comprehensive genetic counselling
  • Proven Track Record: Thousands of South African families trust us with their genetic health
  • Multiple Sample Options: Blood, extracted DNA, or simple FTA card blood spot collection

Take the First Step Toward Clarity Today

Don’t let uncertainty about mitochondrial disorders control your family’s future. With our special pricing of only ZAR 6,700, advanced genetic testing has never been more accessible.

Limited Time Offer: This special pricing of ZAR 6,700 (save ZAR 2,650) won’t last forever. Secure your family’s health clarity while this opportunity remains available.

“The clarity we gained from genetic testing changed everything for our family. We finally had answers and a direction for our son’s care.” – Recent Oracle Genomics Patient