Sale!

NDUFAF1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test

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

-28%

If you’re experiencing unexplained neurological symptoms or have a family history of mitochondrial disorders, our NDUFAF1 Gene Mitochondrial Complex I Deficiency Test provides the answers you need. For just ZAR 6,700 (regularly ZAR 9,350), this comprehensive NGS genetic test offers precise detection of mutations that can cause serious energy metabolism issues affecting your brain and muscles. Our test is specifically designed for South African patients who may be struggling with developmental delays, muscle weakness, or neurological concerns without clear diagnosis. With included genetic counselling and nationwide coverage including Johannesburg, Cape Town, and Durban, we make complex genetic testing accessible and understandable. The 3-4 week turnaround provides timely answers, while our expert team ensures you receive compassionate support throughout the process. Trust Oracle Genomics for accurate, reliable genetic testing that puts your health journey 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

NDUFAF1 Gene Test ZAR 6
NDUFAF1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

[wpforms id=”1190″ title=”true” description=”Request a call back”]

Find Answers for Unexplained Neurological Symptoms with NDUFAF1 Gene Testing

When you’re facing mysterious health challenges that affect your energy, muscle function, or neurological development, it can feel overwhelming and isolating. Our NDUFAF1 Gene Mitochondrial Complex I Deficiency Test is designed to provide the clarity you deserve. For South African families dealing with unexplained symptoms, this test represents hope and answers.

Understanding Your NDUFAF1 Gene Test

The NDUFAF1 gene plays a crucial role in your body’s energy production system. When this gene has mutations, it can disrupt mitochondrial complex I – the first step in your cells’ energy-making process. This disruption can lead to mitochondrial complex I deficiency, affecting how your brain, muscles, and organs function.

Our Next-Generation Sequencing (NGS) technology examines your NDUFAF1 gene with exceptional accuracy, identifying even subtle changes that might be causing your symptoms. This isn’t just a test – it’s a pathway to understanding your body’s unique energy needs.

Who Should Consider This Test?

This test is particularly important if you or your loved one experiences:

  • Unexplained developmental delays in children
  • Progressive muscle weakness or fatigue
  • Neurological symptoms without clear diagnosis
  • Family history of mitochondrial disorders
  • Exercise intolerance or poor stamina
  • Vision or hearing problems of unknown origin
  • Metabolic abnormalities detected in previous tests

Many South African patients have found answers through this testing when other investigations came back inconclusive.

Why Early Detection Matters for Your Health

Identifying NDUFAF1 gene mutations early can significantly impact your health journey:

  • Personalised Treatment Plans: Knowing the specific genetic cause allows for targeted management strategies
  • Family Planning Guidance: Understand inheritance patterns for future family decisions
  • Symptom Management: Develop strategies to manage energy levels and neurological symptoms
  • Peace of Mind: End the uncertainty and diagnostic odyssey
  • Proactive Health Monitoring: Regular check-ups focused on potential complications

Understanding Your Results with Compassion

We know waiting for genetic test results can be anxiety-provoking. Our process is designed to support you every step of the way:

Genetic Counselling Included: Before testing, you’ll meet with our genetic counsellor who will create a family pedigree chart and help you understand what the test might reveal.

Clear Result Interpretation: Your results will be explained in straightforward language, with guidance on what they mean for your health.

Ongoing Support: We provide resources and referrals to specialists who understand mitochondrial disorders.

3-4 Week Turnaround: While comprehensive testing takes time, we work efficiently to provide your results within this timeframe.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
NDUFAF1 Gene Test with Genetic Counselling ZAR 9,350 ZAR 6,700 ZAR 2,650

Price includes genetic counselling session, comprehensive testing, and detailed result interpretation.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Serving patients across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Expert Neurological Specialisation: Tests reviewed by qualified neurologists
  • Advanced NGS Technology: Latest genetic sequencing for maximum accuracy
  • Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
  • Comprehensive Support: From initial counselling to result explanation
  • South African Focus: Understanding local healthcare needs and challenges

Take the First Step Toward Answers Today

Don’t let unexplained symptoms control your life. With our special pricing of ZAR 6,700, now is the perfect time to get the answers you need.



Limited Time Offer: This special pricing of ZAR 6,700 (regularly ZAR 9,350) won’t last forever. Take action now to secure your comprehensive genetic testing.

Convenient Nationwide Access: Whether you’re in Johannesburg, Cape Town, Durban, or anywhere in South Africa, we make genetic testing accessible and supportive.