Find Answers for Unexplained Neurological Symptoms
When your child struggles with developmental delays, muscle weakness, or unexplained neurological symptoms, the uncertainty can be overwhelming. Our NDUFAF4 Gene Mitochondrial Complex I Deficiency Test provides the clarity you need to understand these complex health challenges and create an effective management plan for your family’s wellbeing.
Understanding the NDUFAF4 Genetic Test
This advanced Next-Generation Sequencing (NGS) test specifically examines the NDUFAF4 gene, which plays a crucial role in your body’s energy production system. When this gene has mutations, it can disrupt mitochondrial function, leading to complex I deficiency – a condition that affects how your cells generate energy. Our test provides precise identification of these genetic variations, giving you definitive answers about this rare but serious condition.
Who Should Consider This Test?
This test is particularly important if you or your child experience:
- Unexplained muscle weakness or fatigue
- Developmental delays in childhood
- Neurological symptoms without clear diagnosis
- Family history of mitochondrial disorders
- Exercise intolerance or poor stamina
- Multiple organ system involvement
Early detection through genetic testing can help guide appropriate medical management and improve quality of life outcomes.
Why This Test Matters for Your Family’s Health
Getting a definitive diagnosis through our NDUFAF4 test provides multiple benefits:
- Peace of Mind: End the uncertainty and get clear answers about your health concerns
- Personalised Care: Enable healthcare providers to create targeted treatment plans
- Family Planning: Understand inheritance patterns for future family decisions
- Early Intervention: Access appropriate therapies and management strategies sooner
- Reduced Medical Costs: Avoid unnecessary tests and treatments through accurate diagnosis
Understanding Your Test Results
Our comprehensive approach includes professional genetic counselling to help you understand your results. We’ll explain what any identified genetic variations mean for your health and provide guidance on next steps. Whether your results show a positive identification or rule out NDUFAF4-related disorders, you’ll have the information needed to make confident healthcare decisions with your medical team.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| NDUFAF4 Gene Test | R6,700 | |
| Genetic Counselling Session | INCLUDED | |
| Family Pedigree Analysis | INCLUDED | |
| Results Interpretation | INCLUDED | |
Complete package includes everything needed for comprehensive genetic assessment
Why Trust Oracle Genomics?
- Nationwide Coverage: Serving patients across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Excellence: Partnering with leading neurologists and genetic specialists
- Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
- Compassionate Care: Understanding the emotional journey of genetic testing
- Quick Turnaround: Results typically available within 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple FTA card blood drop
Take Control of Your Health Journey Today
Don’t let uncertainty about neurological symptoms continue to worry you. Our NDUFAF4 genetic test provides the answers you need to move forward with confidence.
Limited Time Offer: Save R2,650 on comprehensive NDUFAF4 testing. Book your appointment today to secure this special pricing and begin your journey to clarity and better health management.
