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SURF1 Gene Leigh Syndrome Due to COX Deficiency NGS Genetic DNA Test

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

-28%

Facing concerns about Leigh syndrome or mitochondrial disorders in your family? Our SURF1 Gene Leigh Syndrome NGS Genetic DNA Test provides definitive answers and peace of mind. For just ZAR 6,700 (regularly ZAR 9,350), this comprehensive test uses advanced Next-Generation Sequencing technology to detect COX deficiency mutations with exceptional accuracy. Whether you’re experiencing neurological symptoms or have a family history of mitochondrial disease, this test offers clarity and empowers informed healthcare decisions. Our process includes professional genetic counselling to help you understand your results and implications for family planning. With nationwide coverage across Johannesburg, Cape Town, Durban, and Pretoria, accessing this life-changing genetic insight has never been more convenient. Take control of your genetic health journey today.

📞 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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SURF1 Gene Leigh Syndrome DNA Test | ZAR 6
SURF1 Gene Leigh Syndrome Due to COX Deficiency NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity About Leigh Syndrome and Mitochondrial Health

When neurological symptoms appear or family history raises concerns about mitochondrial disorders, the uncertainty can be overwhelming. Our SURF1 Gene Leigh Syndrome NGS Genetic DNA Test provides the definitive answers you need to move forward with confidence and peace of mind.

Understanding Your SURF1 Gene Test

This advanced genetic test specifically examines the SURF1 gene, which plays a crucial role in mitochondrial function. When mutations occur in this gene, it can lead to COX (cytochrome c oxidase) deficiency, causing Leigh syndrome – a severe neurological disorder that typically appears in infancy or early childhood.

Using Next-Generation Sequencing (NGS) technology, we analyse your DNA with exceptional precision to identify any mutations that could affect your mitochondrial health. This isn’t just a test – it’s a pathway to understanding your genetic blueprint and making informed decisions about your health journey.

Who Should Consider This Genetic Test?

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

  • Unexplained neurological symptoms or developmental delays
  • Family history of Leigh syndrome or mitochondrial disorders
  • Progressive loss of motor skills or muscle weakness
  • Breathing difficulties or feeding problems in infancy
  • Seizures or movement disorders without clear cause
  • Planning for pregnancy with family history of mitochondrial disease

Early detection through genetic testing can guide appropriate medical management and provide clarity for family planning decisions.

Why This Test Matters for Your Family’s Health

Getting definitive answers about SURF1 gene mutations offers profound benefits:

  • Peace of Mind: Eliminate uncertainty about genetic risks
  • Early Intervention: Guide appropriate medical care and management
  • Family Planning: Make informed decisions about future pregnancies
  • 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 understand that waiting for genetic test results can be anxiety-provoking. Our comprehensive approach includes:

  • Clear Reporting: Easy-to-understand results with professional interpretation
  • Genetic Counselling Session: Included with your test to explain findings and implications
  • Family Pedigree Analysis: Mapping your family history to understand inheritance patterns
  • Follow-up Guidance: Recommendations for next steps and specialist referrals if needed

Our team ensures you never feel alone in understanding your genetic health information.

Affordable Genetic Testing with Exceptional Value

Test Feature Details Value
Regular Price ZAR 9,350 Comprehensive genetic analysis
Special Price ZAR 6,700 Limited time savings of ZAR 2,650
Turnaround Time 3-4 Weeks Prompt results for timely decisions
Sample Type Blood, Extracted DNA, or Blood on FTA Card Convenient collection options
Included Services Genetic Counselling + Family Pedigree Analysis ZAR 1,500+ value included

Why Trust Oracle Genomics?

As South Africa’s leading genetic testing provider, we bring you:

  • 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 unparalleled accuracy
  • Patient-Centred Care: Empathetic support throughout your testing journey
  • Proven Accuracy: Reliable results you can trust for life-changing decisions

Take the First Step Toward Genetic Clarity

Don’t let uncertainty about mitochondrial health create unnecessary anxiety. With our special pricing of only ZAR 6,700, comprehensive genetic testing is more accessible than ever.

Book Your Test Today: Contact our genetic counselling team to schedule your test and begin your journey to understanding your genetic health.

Limited special pricing available – secure your peace of mind while saving ZAR 2,650

Available at testing centres nationwide including Johannesburg, Cape Town, Durban, and Pretoria.