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Williams Syndrome FISH Microdeletion Detection Test

Original price was: R4,000.Current price is: R2,850.

-29%

The Williams Syndrome FISH Microdeletion Detection Test provides crucial early diagnosis for families concerned about developmental delays and heart conditions in their children. For only ZAR 2,850 (regularly ZAR 4,000), this advanced genetic test offers peace of mind through precise detection of the specific chromosome 7 microdeletion associated with Williams Syndrome. Our South African medical team understands the anxiety parents face when their child shows developmental concerns, which is why we’ve made this reliable testing accessible nationwide. With results in just 4 working days and samples accepted daily until 4 pm, you can get the answers you need quickly. Trust Oracle Genomics for accurate, compassionate genetic testing that puts your family’s health first.

📞 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

Williams Syndrome FISH Test ZAR 2
Williams Syndrome FISH Microdeletion Detection Test
R4,000 Original price was: R4,000.R2,850Current price is: R2,850.

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Find Clarity for Your Child’s Development with Williams Syndrome Testing

When you notice your child struggling with developmental milestones or showing unusual facial features, the uncertainty can be overwhelming. As South African parents, you deserve clear answers and compassionate care. Our Williams Syndrome FISH Microdeletion Detection Test provides the definitive diagnosis you need to understand your child’s unique needs and create the best possible care plan.

Understanding the Williams Syndrome FISH Test

The FISH (Fluorescence In Situ Hybridization) test is a highly accurate genetic method that specifically looks for a small missing piece (microdeletion) on chromosome 7. This precise deletion causes Williams Syndrome, a rare genetic condition that affects about 1 in 7,500 to 20,000 people worldwide. Unlike general genetic screens, this targeted approach gives you definitive answers about whether your child has this specific condition.

Our medical team in South Africa uses this advanced technology to provide reliable results that help guide your child’s healthcare journey with confidence.

Who Should Consider This Test?

This test is recommended if your child shows any of these signs that might indicate Williams Syndrome:

  • Developmental delays in walking, talking, or learning
  • Distinctive facial features (broad forehead, short nose, full cheeks)
  • Heart murmurs or cardiovascular concerns
  • Unusual friendliness and lack of stranger anxiety
  • Feeding difficulties in infancy
  • Hypercalcemia (high calcium levels)
  • Family history of genetic conditions

Many South African families find relief in getting clear answers rather than living with uncertainty about their child’s development.

Why Early Detection Matters for Your Child’s Health

Getting an early, accurate diagnosis of Williams Syndrome can significantly improve your child’s quality of life by:

  • Enabling early intervention with speech, physical, and occupational therapy
  • Identifying and monitoring potential heart conditions before they become serious
  • Creating tailored educational plans that address specific learning needs
  • Managing calcium levels and other medical concerns proactively
  • Connecting you with support networks and resources for Williams Syndrome families
  • Reducing parental stress and uncertainty about your child’s future

Early diagnosis means early support – giving your child the best possible start in life.

Understanding Your Test Results

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

  • Positive Result: Confirms Williams Syndrome diagnosis, allowing you to immediately access appropriate medical care and support services
  • Negative Result: Rules out Williams Syndrome, helping your doctor investigate other potential causes for symptoms
  • Inconclusive Result: Rare, but if it occurs, we provide immediate follow-up testing and genetic counseling

Every result comes with guidance from our genetic specialists who understand the South African healthcare landscape and can help you navigate next steps.

Affordable, Accessible Genetic Testing for South African Families

Test Option Price Savings
Special Price ZAR 2,850 Save ZAR 1,150
Regular Price ZAR 4,000

Considering the lifelong benefits of early diagnosis and proper management, this test represents excellent value for your family’s health investment.

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Serving families across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Fast Turnaround: Samples accepted daily until 4 pm, with results in just 4 working days
  • Medical Expertise: Specialised pediatric genetic testing interpreted by experienced professionals
  • Accuracy Guarantee: Advanced FISH technology ensures reliable, definitive results
  • Compassionate Care: We understand the emotional journey of genetic testing and provide supportive guidance

Take the First Step Toward Understanding Your Child’s Health

Don’t let uncertainty about your child’s development create unnecessary stress. With our special pricing of ZAR 2,850, now is the perfect time to get the answers you need.


Important Preparation: Please ensure you bring the duly filled Chromosome & FISH analysis Requisition Form (Form 17) with your 5 mL blood sample collected in a Green Top Sodium Heparin tube.

Take control of your child’s health journey today. Contact Oracle Genomics for compassionate, accurate genetic testing you can trust.