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NDUFA12 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 NDUFA12 Gene Leigh Syndrome NGS Genetic DNA Test provides definitive answers with 99.9% accuracy. For just ZAR 6,700 (regularly ZAR 9,350), this comprehensive test detects mitochondrial complex I deficiency through advanced Next Generation Sequencing technology. We understand the anxiety surrounding rare genetic conditions and provide compassionate genetic counselling to guide you through the process. With nationwide coverage across South Africa including Johannesburg, Cape Town, and Durban, we make expert genetic testing accessible to every family. Early detection can help manage symptoms and improve quality of life. Trust Oracle Genomics for reliable results and professional support throughout your genetic health journey.

📞 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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NDUFA12 Leigh Syndrome DNA Test | ZAR 6
NDUFA12 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 Answers for Mitochondrial Complex I Deficiency

When neurological symptoms appear in your family, the uncertainty can be overwhelming. Our NDUFA12 Gene Leigh Syndrome genetic test provides the clarity you need to understand and manage mitochondrial complex I deficiency. We understand the emotional journey you’re facing and are here to provide compassionate, accurate genetic testing with professional support every step of the way.

Understanding Your NDUFA12 Genetic Test

This advanced Next Generation Sequencing (NGS) test specifically examines the NDUFA12 gene for mutations that cause Leigh syndrome, a severe neurological disorder affecting mitochondrial function. Mitochondria are the energy powerhouses of your cells, and when complex I doesn’t function properly, it can lead to progressive neurological deterioration. Our test provides definitive answers with 99.9% accuracy, giving you the information needed to make informed healthcare decisions.

Who Should Consider This Genetic Test?

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

  • Progressive neurological deterioration in infancy or childhood
  • Developmental regression or loss of motor skills
  • Muscle weakness, poor muscle tone, or movement disorders
  • Breathing difficulties or respiratory problems
  • Family history of mitochondrial disorders or Leigh syndrome
  • Unexplained neurological symptoms in multiple family members

Early detection through genetic testing can help guide treatment approaches and provide crucial information for family planning decisions.

Why Early Detection Matters for Your Family’s Health

Getting tested for NDUFA12 mutations offers significant benefits:

  • Peace of Mind: Eliminate uncertainty about your genetic status
  • Early Intervention: Begin appropriate management strategies sooner
  • Family Planning: Make informed decisions about having children
  • Treatment Guidance: Help healthcare providers develop targeted care plans
  • Genetic Counselling: Understand inheritance patterns and risks for other family members

Understanding Your Test Results

We know waiting for genetic test results can be stressful. Our team provides comprehensive support throughout the process:

  • Clear Results: Easy-to-understand report explaining your genetic status
  • Genetic Counselling: Professional guidance to interpret results and implications
  • Family Pedigree Analysis: Detailed family history mapping to understand inheritance patterns
  • Follow-up Support: Connection to appropriate medical specialists if needed
  • Ongoing Resources: Access to educational materials and support networks

Your results will be available within 3-4 weeks, and we’ll guide you through every step of understanding what they mean for your health.

Affordable Genetic Testing with Exceptional Value

Test Option Regular Price Special Price Savings
NDUFA12 Leigh Syndrome NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

What’s Included:

  • Comprehensive NGS genetic analysis
  • Professional genetic counselling session
  • Family pedigree chart development
  • Detailed results interpretation
  • Nationwide sample collection
  • Ongoing support and resources

Why Trust Oracle Genomics?

We’re committed to providing South Africans with accessible, reliable genetic testing:

  • Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Expert Team: Working with qualified neurologists and genetic specialists
  • Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
  • Multiple Sample Options: Blood, extracted DNA, or simple FTA card blood drop
  • Comprehensive Preparation: Includes clinical history review and genetic counselling
  • Proven Accuracy: 99.9% detection rate for NDUFA12 mutations

Take Control of Your Genetic Health Today

Don’t let uncertainty about mitochondrial disorders control your family’s future. Early detection through genetic testing provides the answers you need to make informed health decisions.

Limited Time Offer: Save ZAR 2,650 on your NDUFA12 genetic test – now only ZAR 6,700

Convenient Testing: Multiple sample collection options available nationwide

Professional Support: Genetic counselling included with every test

Ready to Get Started?

Option 1: Call our genetic counselling team to discuss your concerns and schedule your test

Option 2: Visit one of our nationwide collection centres for sample collection

Option 3: Request a home collection kit for maximum convenience

Take the first step toward understanding your genetic health. Contact Oracle Genomics today and get the answers your family deserves.