Peace of Mind for Your Baby’s Chromosomal Health
When you’re navigating pregnancy concerns or postnatal questions about your baby’s development, the uncertainty can feel overwhelming. Our FISH test for Chromosome 13 and 21 abnormalities provides the clarity and confidence South African parents deserve. This advanced diagnostic tool detects Trisomy 13 and Trisomy 21 with exceptional accuracy, giving you and your healthcare team the information needed to make informed decisions about your family’s health journey.
Understanding the FISH Chromosome Test
The FISH (Fluorescence In Situ Hybridisation) test is a sophisticated chromosomal analysis that specifically examines chromosomes 13 and 21 for abnormalities. Unlike standard chromosome tests, FISH provides rapid, targeted results by using fluorescent probes that bind to specific chromosomal regions. This technology allows our specialists to detect extra copies of these chromosomes – conditions known as Trisomy 13 (Patau syndrome) and Trisomy 21 (Down syndrome) – with remarkable precision.
This test serves as a crucial screening tool that works alongside comprehensive chromosome analysis, offering early detection when timing matters most for your family’s healthcare decisions.
Who Should Consider This Test?
This test is particularly important for:
- Expectant mothers with abnormal ultrasound findings suggesting chromosomal concerns
- Women with advanced maternal age (35 years or older) during pregnancy
- Families with previous chromosomal abnormalities in their medical history
- Parents concerned about specific symptoms in their newborn that may indicate chromosomal conditions
- Couples with abnormal prenatal screening results requiring definitive diagnosis
- Healthcare providers seeking rapid confirmation of suspected chromosomal disorders
If you’re experiencing anxiety about your baby’s development or have received concerning screening results, this test provides the definitive answers you need.
Why Early Detection Matters for Your Family
Choosing chromosomal testing represents a proactive step toward understanding and managing your family’s health. The benefits extend far beyond simple diagnosis:
- Informed Decision-Making: Receive clear, accurate information to guide your healthcare choices
- Early Intervention Planning: When needed, early detection allows for timely medical interventions and support services
- Reduced Anxiety: Replace uncertainty with knowledge and appropriate care planning
- Family Preparation: Understand what to expect and connect with relevant support networks
- Comprehensive Care Coordination: Work with your healthcare team to develop the best possible care plan
Many South African families find that knowing – even when facing challenging news – provides the foundation for accessing appropriate support and moving forward with confidence.
Understanding Your Test Results
We understand that waiting for results can be stressful. Our team provides clear, compassionate explanations of your findings:
- Normal Results: No abnormalities detected in chromosomes 13 and 21 – providing reassurance about these specific conditions
- Abnormal Results: Detection of Trisomy 13 or Trisomy 21, with detailed explanation of what this means for your family
- Professional Guidance: Every result comes with access to genetic counselling and support resources
- Next Steps: Clear recommendations for follow-up care and additional testing if needed
Remember: Knowledge empowers you to make the best decisions for your family’s unique situation, and our team is here to support you through every step.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Turnaround Time |
|---|---|---|---|
| FISH Chromosome 13 & 21 Test | ZAR 2,350 | 10-12 days |
What’s Included: Comprehensive testing, detailed results report, genetic counselling support, and nationwide accessibility across our Johannesburg, Cape Town, Durban and Pretoria locations.
Considering the lifelong impact of chromosomal conditions, this investment in early detection represents significant value for your family’s health and peace of mind.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing facilities in major centres including Johannesburg, Cape Town, Durban and Pretoria
- Medical Expertise: Specialist geneticists and certified laboratory professionals
- Advanced Technology: State-of-the-art FISH methodology with proven accuracy
- Compassionate Care: Understanding the emotional journey of chromosomal testing
- Rapid Results: 10-12 day turnaround without compromising accuracy
- Integrated Support: Connection to genetic counselling and family support services
We’ve helped thousands of South African families navigate chromosomal health concerns with dignity, respect and medical excellence.
Take the Next Step Toward Clarity
Don’t let uncertainty about your baby’s chromosomal health create unnecessary stress. The answers you need are within reach, and our team is ready to support you with professional, compassionate care.
Convenient Nationwide Access: Whether you’re in Johannesburg, Cape Town, Durban, Pretoria or surrounding areas, we make advanced chromosomal testing accessible to South African families when they need it most.