Understanding NDUFAF3 Leigh Syndrome Genetic Testing
When you’re worried about neurological symptoms or have a family history of Leigh syndrome, the uncertainty can feel overwhelming. Our NDUFAF3 Gene Leigh Syndrome NGS Genetic DNA Test is designed to provide the answers and peace of mind you deserve. This advanced genetic test specifically examines the NDUFAF3 gene for mutations that can cause Leigh syndrome – a serious neurological condition that typically appears in infancy or early childhood.
What This Test Detects
The NDUFAF3 gene plays a crucial role in mitochondrial function, and mutations in this gene can disrupt energy production in cells, particularly affecting the brain and nervous system. Our Next Generation Sequencing technology provides comprehensive analysis of this gene, identifying even subtle genetic variations that could indicate Leigh syndrome risk.
Who Should Consider This Test
This test is particularly important if you or your child experience:
- Developmental delays or regression in motor skills
- Muscle weakness or poor muscle tone
- Seizures or episodes of lactic acidosis
- Vision or hearing problems
- Family history of mitochondrial disorders
- Unexplained neurological symptoms in infancy or childhood
Why Early Detection Matters for Your Family’s Health
Early identification of NDUFAF3 gene mutations can be life-changing. Understanding your genetic status allows for:
- Proactive management and treatment planning
- Informed family planning decisions
- Early intervention strategies
- Reduced diagnostic uncertainty and anxiety
- Connection with appropriate specialist care
Understanding Your Results with Compassion
We know that waiting for genetic test results can be stressful. Our team provides clear, compassionate explanations of your results, whether they indicate a mutation or provide reassuring negative findings. Every result comes with guidance on next steps and access to genetic counselling if needed.
Transparent Pricing – Exceptional Value
| Test Option | Price | Savings |
|---|---|---|
| Regular Price | ZAR 9,350 | – |
| Special Price | ZAR 6,700 | ZAR 2,650 |
This represents exceptional value compared to the potential costs of undiagnosed neurological conditions and provides peace of mind that’s truly priceless.
Nationwide Accessibility
We’re proud to serve patients across South Africa with convenient testing locations in:
- Johannesburg and surrounding areas
- Cape Town and Western Cape region
- Durban and KwaZulu-Natal
- Pretoria and Gauteng province
- Plus many other locations nationwide
Trust and Professional Excellence
At Oracle Genomics, we combine cutting-edge NGS technology with compassionate patient care. Our neurological genetic testing is conducted by experienced specialists who understand the sensitive nature of genetic testing for families.
Take Action for Your Family’s Health Today
Don’t let uncertainty about neurological symptoms continue to cause worry. Early detection through our NDUFAF3 Leigh Syndrome genetic test can provide the clarity you need to make informed health decisions.
Book your test today and take the first step toward understanding your genetic health. Our team is ready to support you through this important journey with the professionalism and compassion you deserve.
Test Details: Results typically available within 3-4 weeks | Sample: Blood, Extracted DNA, or Blood on FTA Card | Preparation: Clinical history and genetic counselling session recommended
