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C12ORF65 Gene Combined Oxidative Phosphorylation Deficiency Type 7 NGS Genetic DNA Test

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

-28%

Facing unexplained neurological symptoms or developmental delays in your family? Our C12ORF65 gene test provides definitive answers for combined oxidative phosphorylation deficiency type 7, a serious mitochondrial disorder. Using advanced NGS technology, we deliver 99.9% accurate results to help you understand your genetic health. For just ZAR 6,700 (regularly ZAR 9,350), you gain access to comprehensive genetic analysis that can guide treatment decisions and family planning. Our test is especially crucial for South African families experiencing muscle weakness, vision problems, or developmental regression. With nationwide coverage including Johannesburg, Cape Town, and Durban, we make expert genetic testing accessible to all South Africans. Take control of your family’s 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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C12ORF65 Gene Test | ZAR 6
C12ORF65 Gene Combined Oxidative Phosphorylation Deficiency Type 7 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Answers for Unexplained Neurological Symptoms with C12ORF65 Gene Testing

When your family faces mysterious health challenges like developmental delays, muscle weakness, or vision problems, the uncertainty can be overwhelming. Our C12ORF65 gene test provides the clarity you need to understand combined oxidative phosphorylation deficiency type 7 – a serious mitochondrial disorder that affects energy production in your body’s cells. Using cutting-edge NGS technology, we deliver precise results that can transform your family’s health journey.

Understanding the C12ORF65 Gene Test

This advanced genetic test examines the C12ORF65 gene for mutations that cause combined oxidative phosphorylation deficiency type 7. This condition disrupts your body’s ability to produce energy efficiently, leading to progressive neurological symptoms. Our Next-Generation Sequencing (NGS) technology provides comprehensive analysis with 99.9% accuracy, giving you reliable answers about this inherited condition.

Unlike basic genetic tests, our NGS approach examines the entire gene sequence, ensuring no mutation goes undetected. This thorough analysis is essential for accurate diagnosis and proper management of this complex disorder.

Who Should Consider This Test?

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

  • Unexplained developmental delays in children
  • Progressive muscle weakness or loss of coordination
  • Vision problems or optic atrophy
  • Learning difficulties or intellectual disability
  • Family history of similar neurological symptoms
  • Multiple affected family members suggesting inheritance patterns

Many South African families have found answers through this test when traditional medical evaluations provided incomplete explanations.

Why Early Detection Matters for Your Health

Getting tested for C12ORF65 mutations offers life-changing benefits:

  • Accurate Diagnosis: End the diagnostic odyssey and get definitive answers
  • Personalised Treatment: Guide medical management based on your specific genetic profile
  • Family Planning: Make informed decisions about future pregnancies
  • Early Intervention: Start appropriate therapies before symptoms progress
  • Peace of Mind: Reduce anxiety by understanding your genetic status

Early detection can significantly improve quality of life and help prevent complications associated with this progressive disorder.

Understanding Your Test Results

We understand that waiting for genetic test results can be stressful. Our team provides clear, compassionate explanations of your results:

  • Positive Result: Indicates a mutation in the C12ORF65 gene. Our genetic counsellors will explain what this means for your health and provide guidance on next steps
  • Negative Result: No disease-causing mutations were found, providing reassurance about this specific condition
  • Uncertain Variant: Sometimes we find genetic changes with unknown significance. We’ll explain what this means and recommend appropriate follow-up

Every result includes a comprehensive consultation with our genetic specialists to ensure you fully understand the implications for your health and family.

Affordable Genetic Testing for South African Families

Test Feature Details Value
Regular Price ZAR 9,350 Comprehensive analysis
Special Price ZAR 6,700 Limited time offer
Turnaround Time 3-4 weeks Fast, reliable results
Sample Type Blood, DNA, or FTA Card Convenient options
Technology NGS Gold standard accuracy

Considering the potential healthcare costs of undiagnosed mitochondrial disorders, this test represents excellent value for your family’s health investment.

Why Trust Oracle Genomics?

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

  • Nationwide Coverage: Testing available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Expert Team: Board-certified geneticists and counsellors
  • Advanced Technology: State-of-the-art NGS laboratory
  • Patient Support: Compassionate guidance throughout your journey
  • Proven Accuracy: 99.9% detection rate for genetic mutations

Thousands of South African families have trusted us with their genetic health needs.

Take the First Step Toward Answers

Don’t let uncertainty about neurological symptoms control your family’s future. Our C12ORF65 gene test provides the clarity you need to make informed health decisions.

Limited Time Offer: Book your test at the special price of ZAR 6,700 (regularly ZAR 9,350) – saving you ZAR 2,650



“Getting the C12ORF65 test gave our family the answers we’d been searching for years. The Oracle Genomics team supported us every step of the way.” – Maria K., Cape Town

Test Preparation Requirements

To ensure accurate results, please bring:

  • Complete clinical history of the patient
  • Information for genetic counselling session
  • Family pedigree chart showing affected relatives

Our genetic counsellors will help you prepare all necessary documentation.