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ALG2 Gene Glycosylation Disorder Type 1I NGS Genetic DNA Test

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

-28%

Facing concerns about inherited metabolic disorders? Our ALG2 Gene Glycosylation Disorder Type 1I NGS Genetic DNA Test provides definitive answers and peace of mind. For just ZAR 6,700 (regularly ZAR 9,350), this advanced test uses Next Generation Sequencing technology to detect mutations in the ALG2 gene that cause Congenital Disorders of Glycosylation. Early detection can help manage symptoms, guide treatment decisions, and provide crucial information for family planning. Our comprehensive approach includes genetic counselling to understand your family history and create a personalised care plan. With results in 3-4 weeks and nationwide coverage across South Africa, we make advanced genetic testing accessible and trustworthy. Take control of your health journey with confidence and clarity.

📞 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

ALG2 Gene Test ZAR 6
ALG2 Gene Glycosylation Disorder Type 1I NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding ALG2 Gene Glycosylation Disorder: Your Path to Clarity and Peace of Mind

When you’re concerned about inherited metabolic conditions affecting your family, the uncertainty can feel overwhelming. Our ALG2 Gene Glycosylation Disorder Type 1I test provides the answers you need to move forward with confidence. Using cutting-edge NGS technology, we offer precise genetic analysis that helps families across South Africa understand their health risks and make informed decisions.

What This Test Detects

The ALG2 gene plays a crucial role in glycosylation – the process of adding sugar molecules to proteins. When mutations occur in this gene, it can lead to Congenital Disorders of Glycosylation Type 1I, a rare metabolic condition that affects multiple body systems. Our test specifically identifies these genetic variations, providing clarity about your genetic makeup and potential health risks.

Using Next Generation Sequencing (NGS) technology, we analyse the entire ALG2 gene with exceptional accuracy, ensuring you receive reliable results you can trust for important health decisions.

Who Should Consider This Test?

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

  • Unexplained developmental delays in infants or children
  • Neurological symptoms including seizures or muscle weakness
  • Feeding difficulties and failure to thrive in early childhood
  • Abnormal blood clotting or bleeding tendencies
  • Liver function abnormalities without clear cause
  • Family history of metabolic disorders or unexplained infant deaths
  • Multiple affected family members with similar symptoms

If you’re planning a family and have concerns about inherited conditions, this test can provide valuable insights for your reproductive decisions.

Why Early Detection Matters for Your Health

Identifying ALG2 gene mutations early can significantly impact health outcomes:

  • Personalised Treatment Plans: Guide appropriate medical management and interventions
  • Family Planning Confidence: Make informed decisions about having children
  • Early Intervention: Implement supportive care before symptoms worsen
  • Reduced Diagnostic Uncertainty: End the search for answers and begin focused care
  • Peace of Mind: Replace anxiety with knowledge and a clear path forward

Understanding Your Results

We know waiting for genetic test results can be stressful. That’s why we provide:

  • Clear, Comprehensive Reports: Easy-to-understand results with detailed explanations
  • Genetic Counselling Support: Professional guidance to help interpret your results
  • Family Implications: Information about what results mean for your relatives
  • Next Steps Guidance: Practical recommendations based on your specific results
  • Ongoing Support: Access to resources and specialists as needed

Your results will be available within 3-4 weeks, and we’ll guide you through every step of understanding what they mean for your health.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
ALG2 Gene Glycosylation Disorder Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Genetic Counselling Session Included at no extra cost
Family Pedigree Analysis Included in comprehensive service

This represents exceptional value compared to the potential costs of undiagnosed metabolic disorders and repeated medical investigations.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Tests supervised by qualified general physicians and genetic specialists
  • Advanced Technology: State-of-the-art NGS technology for maximum accuracy
  • Patient-Centred Care: Empathetic support throughout your testing journey
  • Proven Track Record: Trusted by healthcare professionals and patients nationwide

Simple Testing Process

We make genetic testing straightforward and comfortable:

  • Sample Options: Blood draw, extracted DNA, or simple finger-prick blood spot on FTA card
  • Genetic Counselling: Comprehensive session to understand your family history
  • Family Pedigree: We create a detailed family tree to identify patterns
  • Clinical History Review: Thorough assessment of relevant medical information
  • Convenient Locations: Testing available at multiple centres near you

Take the First Step Toward Clarity

Don’t let uncertainty about genetic health risks control your life. With our special pricing of ZAR 6,700, now is the perfect time to get the answers you deserve.



Limited Time Offer: This special pricing of ZAR 6,700 (save ZAR 2,650) won’t last forever. Secure your peace of mind today.

Convenient Nationwide Access: With testing centres across South Africa, including Johannesburg, Cape Town, Durban and Pretoria, advanced genetic testing is more accessible than ever.