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Fragile X Syndrome (FMR1) Detection by PCR

Original price was: R3,350.Current price is: R2,700.

-19%

Facing concerns about genetic conditions in your family? Our Fragile X Syndrome (FMR1) PCR test provides the clarity you need for just ZAR 2,700. This advanced genetic screening detects the FMR1 gene mutation responsible for Fragile X Syndrome, offering peace of mind for family planning decisions. With results delivered within 3-4 days, you’ll gain valuable insights into your genetic health. Our nationwide testing centres in Johannesburg, Cape Town, and Durban make accessing this crucial test convenient and stress-free. Trust our medical expertise and cutting-edge PCR technology for accurate, reliable results that can guide your healthcare journey with confidence.

📞 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

Fragile X Syndrome PCR Test | ZAR 2
Fragile X Syndrome (FMR1) Detection by PCR
R3,350 Original price was: R3,350.R2,700Current price is: R2,700.

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Find Clarity About Fragile X Syndrome Genetic Risks

When you’re planning a family or concerned about genetic conditions, uncertainty can be overwhelming. Our Fragile X Syndrome (FMR1) PCR test provides the definitive answers you need to make informed decisions about your family’s health future. For just ZAR 2,700, gain the peace of mind that comes from knowing your genetic status with medical-grade accuracy.

Understanding Your Fragile X Syndrome Test

Fragile X Syndrome is the most common inherited cause of intellectual disability and autism spectrum disorders. Our PCR (Polymerase Chain Reaction) test specifically examines the FMR1 gene to detect the genetic mutation responsible for this condition. Using just a small blood sample, we provide precise analysis that helps you understand your genetic risks and make empowered healthcare choices.

The test works by amplifying specific DNA sequences, allowing our medical experts to identify the exact number of CGG repeats in the FMR1 gene – the key indicator for Fragile X Syndrome risk.

Who Should Consider This Genetic Screening?

This test is particularly important if you experience:

  • Family history of intellectual disability or developmental delays
  • Known Fragile X Syndrome in relatives
  • Planning pregnancy and concerned about genetic risks
  • Unexplained fertility issues or premature ovarian insufficiency
  • Personal history of neurological symptoms with unknown cause
  • Family members with tremor/ataxia syndrome (FXTAS)

Early detection through genetic screening can provide crucial information for family planning and proactive healthcare management.

Why This Test Matters for Your Family’s Health

Getting tested for Fragile X Syndrome offers significant benefits:

  • Family Planning Confidence: Make informed decisions about having children with clear understanding of genetic risks
  • Early Intervention: If positive, enables early support and interventions for better outcomes
  • Peace of Mind: Eliminate uncertainty and reduce anxiety about genetic conditions
  • Comprehensive Health Picture: Understand your complete genetic health profile
  • Future Planning: Prepare appropriately for potential healthcare needs

Understanding Your Test Results

We know waiting for genetic test results can be stressful. Our medical team provides clear, compassionate explanations of your results:

  • Normal Result: No FMR1 gene mutation detected – you can proceed with family planning with confidence
  • Carrier Status: You carry the gene but may not show symptoms – important information for genetic counselling
  • Positive Result: FMR1 mutation detected – our genetic counsellors will guide you through next steps

Every result comes with professional guidance and support options to help you understand what it means for your health journey.

Affordable Genetic Testing for South African Families

Test Option Price Turnaround Time
Fragile X Syndrome (FMR1) PCR Test ZAR 2,700 ZAR 3,350 3-4 Days

Note: A doctor’s prescription is required for this test, except for surgery, pregnancy cases, or international travel purposes.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Testing centres conveniently located 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 End Point PCR methodology ensures highest accuracy
  • Quick Results: Receive your comprehensive report within 3-4 days
  • Professional Support: Access to genetic counselling and medical guidance

Take Control of Your Genetic Health Today

Don’t let uncertainty about genetic risks delay your family planning decisions. Our Fragile X Syndrome test provides the clarity you need to move forward with confidence.



Limited Time Offer: Save ZAR 650 on your genetic screening. Book your appointment today and take the first step toward genetic clarity and family health assurance.

Test Preparation & Sample Collection

Sample Type: Peripheral blood (EDTA Vacutainer 2ml)

Method: End Point PCR

Prescription Requirements: Doctor’s prescription required (exceptions for surgery, pregnancy, or international travel)

Our professional phlebotomists make the blood collection process quick and comfortable at any of our nationwide centres.