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MTRR Gene Homocystinuria-Megaloblastic Anemia cbl E Type NGS Genetic DNA Test

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

-28%

Are you concerned about unexplained fatigue, neurological symptoms, or developmental delays in your family? Our MTRR Gene Homocystinuria-Megaloblastic Anemia cbl E Type NGS Genetic DNA Test provides definitive answers about this rare but serious inherited condition. For only R6,700 (regularly R9,350), you’ll receive comprehensive genetic analysis using advanced Next Generation Sequencing technology that detects mutations in the MTRR gene responsible for vitamin B12 metabolism disorders. This test is crucial for families with a history of homocystinuria symptoms like vision problems, intellectual disability, or blood disorders. Our expert team provides genetic counselling to help you understand your family’s risk and create a personalised health management plan. With results delivered within 3-4 weeks and nationwide coverage including Johannesburg, Cape Town, and Durban, you can take control of your family’s genetic health with confidence and peace of mind.

📞 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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MTRR Gene Test R6
MTRR Gene Homocystinuria-Megaloblastic Anemia cbl E Type NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Take Control of Your Genetic Health: MTRR Gene Testing for Homocystinuria and Megaloblastic Anemia

Living with unexplained health symptoms can be overwhelming, especially when they affect your energy levels, neurological function, or your child’s development. If you’ve noticed persistent fatigue, developmental delays, or neurological issues in your family, our advanced MTRR gene testing provides the clarity you need to make informed health decisions.

Understanding Your MTRR Gene Test

The MTRR gene plays a crucial role in how your body processes vitamin B12, which is essential for healthy blood cell formation and proper neurological function. When this gene contains mutations, it can lead to two serious conditions: homocystinuria (affecting multiple body systems) and megaloblastic anemia (affecting blood cell production).

Our Next Generation Sequencing (NGS) technology examines your MTRR gene with exceptional accuracy, identifying even the smallest genetic variations that could impact your health. This isn’t just a test – it’s a comprehensive genetic assessment that provides definitive answers about your inherited risk factors.

Who Should Consider This Genetic Test?

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

  • Unexplained fatigue and weakness that doesn’t improve with rest
  • Developmental delays in children or learning difficulties
  • Neurological symptoms like numbness, tingling, or coordination problems
  • Vision problems or eye abnormalities
  • Family history of blood disorders or metabolic conditions
  • Unexplained anemia that doesn’t respond to standard treatments
  • Skeletal abnormalities or unusual body proportions

Early detection through genetic testing can transform health outcomes and provide opportunities for proactive management.

Why This Test Matters for Your Family’s Health

Getting tested provides more than just answers – it offers peace of mind and actionable health information:

  • Early Intervention: Identify risks before symptoms become severe
  • Personalised Treatment: Guide vitamin B12 therapy and dietary management
  • Family Planning: Understand inheritance patterns for future generations
  • Prevent Complications: Reduce risk of stroke, vision loss, and developmental issues
  • End Diagnostic Uncertainty: Stop the cycle of unexplained symptoms and misdiagnoses

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. That’s why we provide comprehensive support throughout the process:

Clear, Understandable Reports: Your results will be presented in easy-to-understand language with clear explanations of what they mean for your health.

Expert Genetic Counselling: Before testing, our genetic counsellors help create a detailed family history to better understand your specific risk factors.

Personalised Guidance: We explain how your results impact treatment options, lifestyle adjustments, and family health planning.

Ongoing Support: We’re here to answer your questions and help you navigate next steps with confidence.

Affordable Genetic Testing with Exceptional Value

Service Regular Price Special Price Savings
MTRR Gene NGS Test R9,350 R6,700 R2,650
Genetic Counselling Session Included at no extra cost
Family Pedigree Analysis Included at no extra cost
Results Interpretation Included at no extra cost

Consider the long-term value: Early detection can prevent costly medical complications and provide years of better health management.

Why Trust Oracle Genomics?

Nationwide Coverage: Accessible testing centres across South Africa including Johannesburg, Cape Town, Durban, and Pretoria

Medical Expertise: Our tests are supervised by qualified general physicians and genetic specialists

Advanced Technology: Using cutting-edge NGS technology for the most accurate results available

Multiple Sample Options: Choose from blood draw, extracted DNA, or simple finger-prick blood spot on FTA card

Reliable Turnaround: Results delivered within 3-4 weeks with ongoing support

Patient-Focused Care: We prioritise your comfort, understanding, and peace of mind throughout the testing journey

Take the First Step Toward Genetic Clarity

Don’t let uncertainty about your genetic health create unnecessary anxiety. With our special pricing of R6,700 and comprehensive support services, there’s never been a better time to gain the clarity you deserve.



Limited Time Offer: This special pricing of R6,700 (saving you R2,650) won’t last forever. Secure your family’s genetic health information today.

Convenient Nationwide Access: Whether you’re in Johannesburg, Cape Town, Durban, or anywhere in South Africa, we make genetic testing accessible and stress-free.