FISH Prader-Willi Syndrome SNRPN Test: Early Detection for Better Outcomes
We understand the deep concern parents feel when their child shows unusual developmental patterns or feeding difficulties. The FISH Prader-Willi Syndrome test provides the clarity and answers you need to make informed decisions about your child’s health journey. This specialized genetic test offers peace of mind through accurate, reliable detection of Prader-Willi Syndrome, helping you take proactive steps toward proper management and care.
Understanding the FISH Prader-Willi Syndrome Test
The FISH (Fluorescence In Situ Hybridization) Prader-Willi Syndrome SNRPN test is a highly specialized genetic examination that detects specific chromosomal abnormalities on chromosome 15. This advanced technology allows our genetic specialists to identify the missing genetic material that causes Prader-Willi Syndrome, providing definitive answers about your child’s genetic makeup.
Using state-of-the-art FISH methodology, we analyze the SNRPN gene region with 99.9% accuracy, ensuring you receive the most reliable results possible. This test is specifically designed to detect the microdeletions and genetic patterns associated with Prader-Willi Syndrome, giving you the confidence that comes from precise medical testing.
Who Should Consider This Test?
This test is recommended for infants and children showing symptoms that may indicate Prader-Willi Syndrome, including:
- Poor muscle tone (hypotonia) in infancy
- Feeding difficulties and failure to thrive in early months
- Delayed developmental milestones
- Excessive appetite and weight gain in childhood
- Behavioral challenges and learning difficulties
- Short stature and small hands/feet
- Underdeveloped genitalia
If your child exhibits several of these symptoms, early testing can provide the answers needed to begin appropriate interventions and support.
Why Early Detection Matters for Your Child’s Health
Early diagnosis of Prader-Willi Syndrome through our FISH test offers numerous life-changing benefits:
- Early Intervention: Begin specialized therapies and nutritional management sooner
- Improved Quality of Life: Better management of symptoms and complications
- Family Planning: Understand genetic risks for future pregnancies
- Educational Support: Access appropriate learning accommodations early
- Medical Management: Coordinate care with specialists who understand the condition
- Peace of Mind: Replace uncertainty with a clear path forward
Early detection means your child can receive the specialized care they need during critical developmental stages.
Understanding Your Test Results
We know waiting for genetic test results can be stressful. Our team provides clear, compassionate explanations of your results:
- Positive Result: Indicates Prader-Willi Syndrome is present. Our genetic counselors will explain what this means and connect you with appropriate specialists
- Negative Result: Rules out Prader-Willi Syndrome, allowing you to explore other potential causes for symptoms
- Inconclusive Result: Rare cases may require additional testing, which we’ll guide you through
Every result comes with detailed interpretation and next-step recommendations from our experienced genetic specialists.
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| FISH Prader-Willi Syndrome SNRPN Test | ZAR 3,000 | ZAR 2,000 |
Turnaround Time: Sample accepted daily by 4 pm | Results in 4 working days
Sample Requirements: 5 mL (3 mL minimum) whole blood from 1 Green Top (Sodium Heparin) tube. Ship at 18-22°C. DO NOT FREEZE.
Important: Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Specialized pediatric genetic testing with 99.9% accuracy
- Compassionate Care: Understanding the emotional journey of genetic testing
- Fast Results: Quick 4-working-day turnaround for timely decisions
- Professional Standards: Adherence to international genetic testing protocols
Take the First Step Toward Clarity
Don’t let uncertainty about your child’s health create unnecessary stress. Early detection through our FISH Prader-Willi Syndrome test can provide the answers you need to move forward with confidence.
Book your test today and take advantage of our special ZAR 3,000 pricing. Our team is ready to support you through every step of this important health journey.
Limited time special pricing available. Early detection leads to better outcomes.
