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Karyotyping for Detection of Fragile X Syndrome

Original price was: R3,350.Current price is: R2,500.

-25%

Facing concerns about genetic conditions in your family? Our Fragile X Syndrome karyotyping test provides the clarity you need for informed family planning decisions. At just ZAR 2,500 (regularly ZAR 3,350), this comprehensive genetic analysis offers peace of mind and early detection capabilities. Using advanced cell culture techniques, we analyse your chromosomes to identify the fragile X mutation that can cause developmental delays and intellectual disabilities. Whether you’re planning a family, have a family history of genetic conditions, or want reassurance about your genetic health, this test delivers accurate, reliable results within 7-10 days. Available nationwide across South Africa, including Johannesburg, Cape Town, and Durban, our expert team ensures you receive professional care and clear guidance throughout the process. Take control of your genetic health 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 Karyotyping Test | ZAR 2
Karyotyping for Detection of Fragile X Syndrome
R3,350 Original price was: R3,350.R2,500Current price is: R2,500.

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Find Clarity About Fragile X Syndrome with Advanced Karyotyping

When you’re concerned about genetic conditions affecting your family’s future, the uncertainty can feel overwhelming. Our Fragile X Syndrome karyotyping test provides the answers you need to make informed decisions with confidence. Using sophisticated genetic analysis, we help South African families understand their genetic health and plan for the future with peace of mind.

Understanding Fragile X Syndrome Karyotyping

Karyotyping is a specialised genetic test that examines your chromosomes under high magnification to detect abnormalities. For Fragile X Syndrome detection, we specifically look for the fragile site on the X chromosome that indicates this genetic condition. This non-invasive test requires only a small blood sample and provides comprehensive insights into your genetic makeup.

Using advanced cell culture techniques, our laboratory experts grow your cells and analyse them during their division phase, allowing us to identify even subtle chromosomal changes that could indicate Fragile X Syndrome.

Who Should Consider This Important Test?

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

  • Family history of intellectual disabilities or developmental delays
  • Previous children with learning difficulties or autism spectrum features
  • Unexplained infertility or recurrent pregnancy loss
  • Planning pregnancy and wanting genetic screening
  • Known family history of Fragile X Syndrome
  • Concerns about passing genetic conditions to children

Many South Africans are unaware they carry the Fragile X premutation, making this test crucial for proactive family planning.

Why Early Detection Matters for Your Family’s Health

Early identification of Fragile X Syndrome carrier status provides invaluable benefits:

  • Informed Family Planning: Make confident decisions about having children with complete genetic information
  • Early Intervention: If needed, access specialised support and therapies sooner
  • Peace of Mind: Reduce anxiety about unknown genetic risks
  • Financial Planning: Prepare for potential future healthcare needs
  • Medical Management: Work with healthcare providers to create personalised care plans

Understanding Your Test Results

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

  • Normal Result: No fragile X mutation detected – you can proceed with family planning confidently
  • Carrier Status: You carry the premutation but may not show symptoms – important for family planning decisions
  • Affected Result: Fragile X Syndrome detected – we connect you with genetic counselling and support services

Regardless of your results, our genetic counsellors are available to help you understand the implications and next steps.

Affordable Genetic Testing for South African Families

Test Description Regular Price Special Price Savings
Fragile X Syndrome Karyotyping ZAR 3,350 ZAR 2,500 ZAR 850

Price includes comprehensive analysis, detailed report, and genetic counselling consultation if needed.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Expert Team: Qualified genetic specialists and medical professionals
  • Advanced Technology: State-of-the-art laboratory equipment
  • Fast Results: 7-10 day turnaround time
  • Patient-Focused Care: Empathetic support throughout your journey
  • Proven Accuracy: Reliable results you can trust for important life decisions

Take the First Step Toward Genetic Clarity Today

Don’t let uncertainty about genetic health cloud your family planning decisions. With our affordable ZAR 2,500 pricing and nationwide availability, getting the answers you need has never been easier.

Multiple Ways to Book Your Test:

  • Online Booking: Secure, convenient scheduling available 24/7
  • Phone Consultation: Speak directly with our genetic specialists
  • Clinic Visit: Visit our facilities in major cities nationwide
  • Home Collection: Mobile phlebotomy services available in select areas

Important Note: This test requires a doctor’s prescription, except for surgery preparation, pregnancy cases, or travel abroad requirements.

Limited Time Offer: Save ZAR 850 on your Fragile X Syndrome karyotyping. Early detection provides the best opportunities for proactive health management and informed family planning.

Contact Oracle Genomics today and take control of your genetic health journey with confidence and peace of mind.