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RFT1 Gene Glycosylation Disorder Type 1N NGS Genetic DNA Test

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

-28%

Facing concerns about inherited metabolic disorders? Our RFT1 Gene Glycosylation Disorder Type 1N NGS Genetic DNA Test provides definitive answers for South African families. For just ZAR 6,700 (regularly ZAR 9,350), this advanced Next-Generation Sequencing test detects mutations in the RFT1 gene responsible for Congenital Disorders of Glycosylation. We understand the anxiety that comes with potential genetic conditions, which is why our test offers 99.9% accuracy and comprehensive genetic counselling. Available nationwide including Johannesburg, Cape Town, and Durban, our trusted testing process gives you the clarity needed for proper medical management. Early detection can significantly improve quality of life and guide appropriate treatment strategies. Take control of your family’s health journey with confidence through our reliable genetic testing services.

📞 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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RFT1 Gene Test ZAR 6
RFT1 Gene Glycosylation Disorder Type 1N NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity About Glycosylation Disorders with Our RFT1 Gene Test

We understand the worry and uncertainty that comes with potential inherited metabolic conditions. When you’re concerned about developmental delays, neurological symptoms, or family history of genetic disorders, getting clear answers becomes essential for peace of mind and proper healthcare planning.

Understanding Your RFT1 Gene Test

This advanced genetic test examines your RFT1 gene using Next-Generation Sequencing (NGS) technology to identify mutations that cause Glycosylation Disorder Type 1N. Think of it as reading your genetic blueprint with incredible precision – we’re looking for specific spelling errors in your DNA that could affect how your body processes sugars and proteins.

Glycosylation disorders are rare metabolic conditions where the body struggles to properly attach sugar molecules to proteins, which can impact multiple body systems including brain development, liver function, and growth.

Who Should Consider This Genetic Test?

This test brings clarity to families experiencing:

  • Unexplained developmental delays in infants or children
  • Neurological symptoms like seizures or coordination problems
  • Family history of metabolic or genetic disorders
  • Multiple organ system involvement without clear diagnosis
  • Abnormal blood test results suggesting metabolic issues
  • Previous children with similar unexplained health concerns

If you’ve been searching for answers about complex health symptoms in your family, this test could provide the missing piece to your diagnostic puzzle.

Why Early Detection Matters for Your Family’s Health

Getting a definitive diagnosis through genetic testing transforms uncertainty into actionable healthcare:

  • Peace of Mind: Replace anxiety with clear understanding of your genetic status
  • Personalised Care: Guide medical management based on specific genetic findings
  • Family Planning: Make informed decisions about future pregnancies
  • Early Intervention: Access appropriate therapies and treatments sooner
  • Reduced Medical Costs: Avoid unnecessary tests and treatments through accurate diagnosis

Early detection can significantly improve quality of life and treatment outcomes for affected individuals.

Understanding Your Test Results – We’re Here to Guide You

We know waiting for genetic test results can be stressful. That’s why we provide comprehensive support throughout the process:

  • Clear Reporting: Easy-to-understand results with detailed explanations
  • Genetic Counselling: Professional guidance to interpret your results
  • Family Implications: Understanding what results mean for your relatives
  • Next Steps: Clear recommendations for medical follow-up
  • Ongoing Support: Access to genetic specialists for additional questions

Your results will clearly indicate whether RFT1 gene mutations were detected and what this means for your health management.

Transparent Pricing – Investing in Your Family’s Health

Service Regular Price Special Price Savings
RFT1 Gene Glycosylation Disorder Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Turnaround Time 3-4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card

Consider this an investment that could save thousands in future medical costs through accurate diagnosis and targeted treatment.

Why South African Families 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 ensuring 99.9% accuracy
  • Comprehensive Support: Genetic counselling included to help you understand results
  • Proven Reliability: Trusted by healthcare professionals nationwide
  • Patient-Focused: Empathetic care throughout your testing journey

Take the First Step Toward Genetic Clarity Today

Don’t let uncertainty about genetic conditions create unnecessary stress for your family. Our RFT1 gene test provides the answers you need to make informed healthcare decisions.

Multiple Ways to Book Your Test:

  • Online Booking: Secure instant appointment scheduling
  • Telephone Consultation: Speak directly with our genetic specialists
  • Clinic Visit: Personalised service at our nationwide centres
  • Home Collection: Convenient sample collection at your location

Limited Time Special: Save ZAR 2,650 on your RFT1 gene test. Early detection leads to better health outcomes – book your test now while this special pricing is available.

Join thousands of South African families who have found answers and peace of mind through our reliable genetic testing services.