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PHKG2 Gene Glycogen Storage Disease Type 9C NGS Genetic DNA Test

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

-28%

Facing concerns about glycogen storage disorders in your family? Our PHKG2 Gene Glycogen Storage Disease Type 9C NGS Genetic DNA Test provides definitive answers with 99.9% accuracy. For just ZAR 6,700 (regularly ZAR 9,350), you’ll gain peace of mind through advanced Next Generation Sequencing technology. This comprehensive test identifies mutations in the PHKG2 gene that cause glycogen metabolism issues, helping you understand your genetic risk and make informed health decisions. With genetic counselling included and nationwide coverage across South Africa, including Johannesburg, Cape Town, and Durban, we make complex genetic testing accessible and understandable. Early detection can prevent serious complications and guide proper management strategies for you and your family.

📞 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

PHKG2 Gene Test for Glycogen Storage Disease | ZAR 6
PHKG2 Gene Glycogen Storage Disease Type 9C NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Your Genetic Risk for Glycogen Storage Disease Type 9C

When you’re worried about inherited metabolic conditions affecting your family’s health, getting clear answers can feel overwhelming. Our PHKG2 Gene Glycogen Storage Disease Type 9C NGS Genetic DNA Test provides the certainty you need to move forward with confidence. Using cutting-edge Next Generation Sequencing technology, we deliver accurate results that help you understand your genetic makeup and make informed decisions about your health journey.

What This Test Detects

This specialised genetic test examines the PHKG2 gene for mutations that cause Glycogen Storage Disease Type 9C. When this gene doesn’t function properly, your body struggles to break down glycogen into glucose, leading to energy metabolism issues that can affect liver function and muscle development. Our advanced NGS technology provides comprehensive analysis of your genetic code, identifying even the smallest variations that could impact your health.

Who Should Consider This Test

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

  • Unexplained liver enlargement or liver function abnormalities
  • Muscle weakness or developmental delays in children
  • Family history of metabolic disorders or glycogen storage diseases
  • Unexplained fatigue or exercise intolerance
  • Growth delays or failure to thrive in infants and children
  • Previous inconclusive metabolic testing results

If you’re planning a family and have concerns about genetic inheritance, this test provides valuable insights for informed family planning decisions.

Why Early Detection Matters for Your Health

Understanding your genetic status empowers you to take proactive steps toward better health management. Early detection of PHKG2 gene mutations allows for:

  • Personalised treatment and management strategies
  • Prevention of serious complications through early intervention
  • Informed family planning decisions
  • Reduced anxiety through definitive answers
  • Access to appropriate specialist care and support
  • Better understanding of your child’s developmental needs

Peace of mind comes from knowing your genetic status and having a clear path forward for your health journey.

Understanding Your Test Results

We understand that waiting for genetic test results can be stressful. Our comprehensive reporting includes:

  • Clear, easy-to-understand explanation of your results
  • Genetic counselling session to discuss findings and implications
  • Personalised recommendations based on your genetic profile
  • Family pedigree chart showing inheritance patterns
  • Guidance on next steps and specialist referrals if needed
  • Ongoing support for questions and concerns

Our genetic specialists ensure you fully understand your results and what they mean for your health and your family’s wellbeing.

Transparent Pricing and Value

Service Regular Price Special Price Savings
PHKG2 Gene Glycogen Storage Disease Type 9C NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Your investment includes: Comprehensive genetic analysis, genetic counselling session, detailed results report, family pedigree chart, and ongoing support. Compared to potential lifelong health complications, this test represents exceptional value for your family’s health security.

Why Trust Oracle Genomics

We’ve built our reputation on accuracy, empathy, and professional excellence:

  • Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Advanced Technology: Next Generation Sequencing ensures 99.9% accuracy
  • Expert Team: Qualified genetic counsellors and medical professionals
  • Comprehensive Support: From testing to results interpretation and beyond
  • Proven Track Record: Thousands of satisfied patients across South Africa
  • Easy Sample Collection: Blood draw or simple FTA card option available

Take Control of Your Genetic Health Today

Don’t wait for symptoms to appear – proactive genetic testing gives you the power to protect your family’s health. With results in just 3-4 weeks and genetic counselling included, you’ll have the clarity and confidence to make informed health decisions.

Easy Booking Options:

  • Online Booking: Secure online appointment scheduling
  • Telephone Consultation: Speak directly with our genetic specialists
  • Clinic Visit: Visit our conveniently located centres nationwide
  • Home Collection: Mobile phlebotomy services available in major cities

Limited Time Special: Book now to secure your ZAR 6,700 special price before this offer ends. Early detection could save years of uncertainty and prevent serious health complications.

Ready to begin your health journey? Contact Oracle Genomics today at [Phone Number] or visit our website to schedule your genetic counselling session and testing.