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PGAM2 Gene Glycogen Storage Disease Type 10 NGS Genetic DNA Test

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

-28%

Living with unexplained muscle pain, weakness, or exercise intolerance can be frightening and isolating. Our PGAM2 Gene Glycogen Storage Disease Type 10 NGS Genetic DNA Test provides the answers you need for just ZAR 6,700 (regularly ZAR 9,350). This comprehensive genetic test uses advanced NGS technology to identify mutations in the PGAM2 gene that cause Glycogen Storage Disease Type 10. Early detection is crucial for managing symptoms and preventing serious complications. Our test is designed with South African patients in mind, offering nationwide coverage and professional genetic counselling. With results available in just 3-4 weeks, you can take control of your health journey with confidence and clarity. Trust Oracle Genomics for accurate, reliable genetic testing that puts your health first.

📞 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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PGAM2 Gene Test for Glycogen Storage Disease | ZAR 6
PGAM2 Gene Glycogen Storage Disease Type 10 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 Muscle Weakness and Exercise Intolerance

When your body doesn’t respond to exercise the way it should, when muscle pain becomes your constant companion, or when fatigue overwhelms your daily life – it’s time to seek answers. Our PGAM2 Gene Glycogen Storage Disease Type 10 test provides the clarity you deserve, helping you understand your body’s unique challenges and take control of your health journey.

Understanding Your PGAM2 Gene Test

Glycogen Storage Disease Type 10 is a rare genetic condition that affects how your body stores and uses energy. The PGAM2 gene provides instructions for making an enzyme called phosphoglycerate mutase, which is essential for energy production in muscle cells. When this gene has mutations, it can lead to exercise intolerance, muscle pain, and weakness that often goes undiagnosed for years.

Our advanced Next-Generation Sequencing (NGS) technology examines your PGAM2 gene with exceptional accuracy, identifying even the smallest genetic variations that could be affecting your health. This isn’t just a test – it’s a pathway to understanding your body’s unique needs.

Who Should Consider This Test?

If you experience any of these symptoms, this test could provide life-changing answers:

  • Unexplained muscle pain or cramping during or after exercise
  • Exercise intolerance that limits your daily activities
  • Muscle weakness that doesn’t improve with rest
  • Family history of similar symptoms or diagnosed glycogen storage diseases
  • Fatigue that seems disproportionate to your activity level
  • Dark-coloured urine after exercise (myoglobinuria)

Many South Africans struggle with these symptoms without understanding their cause. Early detection can prevent years of frustration and misdiagnosis.

Why Early Detection Matters for Your Health

Getting answers through genetic testing can transform your approach to health and wellness:

  • Personalised Management: Understand exactly what your body needs to manage symptoms effectively
  • Prevent Complications: Early intervention can prevent serious muscle damage and kidney problems
  • Family Planning: Make informed decisions about family health and genetic risks
  • Peace of Mind: End the uncertainty and anxiety of unexplained symptoms
  • Targeted Treatment: Work with your healthcare provider on strategies specifically designed for your condition

Understanding Your Results with Confidence

We understand that waiting for genetic test results can be anxiety-provoking. That’s why we provide clear, comprehensive reports that your healthcare provider can easily interpret. Our results include:

  • Clear explanation of any PGAM2 gene mutations detected
  • Detailed information about what these findings mean for your health
  • Guidance for discussing results with your doctor
  • Recommendations for next steps in your health journey
  • Access to genetic counselling if needed

Remember: A positive result doesn’t define you – it empowers you with knowledge to make the best choices for your health.

Transparent Pricing – Exceptional Value

Test Option Regular Price Special Price Savings
PGAM2 Gene Glycogen Storage Disease Type 10 Test ZAR 9,350 ZAR 6,700 ZAR 2,650

What’s Included:

  • Comprehensive PGAM2 gene analysis using NGS technology
  • Professional genetic counselling session
  • Detailed clinical report
  • 3-4 week turnaround time
  • Multiple sample options (blood, extracted DNA, or blood spot card)
  • Nationwide coverage across South Africa

Why Trust Oracle Genomics?

We’re committed to providing South Africans with accessible, reliable genetic testing:

  • Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
  • Medical Expertise: Tests supervised by qualified general physicians and genetic specialists
  • Advanced Technology: State-of-the-art NGS testing for maximum accuracy
  • Patient-Focused: We understand the emotional journey of genetic testing
  • Proven Track Record: Trusted by healthcare providers across the country

Take the First Step Toward Understanding Your Health

Don’t let unexplained symptoms control your life any longer. With our special pricing of ZAR 6,700, there’s never been a better time to get the answers you deserve.

Limited Time Offer: This special pricing of ZAR 6,700 (regularly ZAR 9,350) won’t last forever. Take advantage of these savings while you can invest in your health future.

“The clarity I gained from this test changed everything. Finally understanding why my body responds differently to exercise has been life-changing.” – Previous Patient

Test Preparation

To ensure the most accurate results, please bring:

  • Your complete clinical history
  • Information about family members affected by similar symptoms
  • Be prepared for a genetic counselling session to create a family pedigree chart

Sample collection is simple and can be done through blood draw, extracted DNA, or a simple blood spot on an FTA card.