Understanding PIGN Syndrome: Your Path to Answers and Peace of Mind
When your child faces multiple congenital anomalies, muscle weakness (hypotonia), or seizures, the uncertainty can be overwhelming. As South African parents, you deserve clear answers and a path forward. Our PIGN Syndrome NGS Genetic DNA Test provides the definitive genetic insights you need to understand your child’s condition and make informed healthcare decisions.
What This Test Reveals About Your Child’s Health
The PIGN gene plays a crucial role in early development, and mutations can lead to Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 1. Our advanced Next-Generation Sequencing (NGS) technology examines the PIGN gene with exceptional accuracy, identifying specific genetic variations that may be causing your child’s symptoms. This isn’t just a test – it’s a comprehensive genetic investigation that provides the clarity South African families need.
Is This Test Right for Your Family?
This test is specifically recommended for children and families experiencing:
- Multiple congenital anomalies present from birth
- Persistent muscle weakness or low muscle tone (hypotonia)
- Recurrent seizures or epilepsy
- Developmental delays or intellectual disability
- Family history of similar symptoms
- Unexplained multiple organ system involvement
If your child’s condition has been difficult to diagnose or you suspect a genetic cause, this test can provide the answers that have been eluding you.
Why Early Genetic Detection Matters for Your Child’s Future
Getting a definitive genetic diagnosis through our PIGN Syndrome test offers life-changing benefits:
- Personalised Treatment Plans: Guide your healthcare team in developing targeted interventions
- Family Planning Insights: Understand inheritance patterns for future family decisions
- Early Intervention Opportunities: Access appropriate therapies and support services sooner
- Reduced Diagnostic Odyssey: End the cycle of multiple tests and specialist visits
- Emotional Closure: Finally understand the “why” behind your child’s symptoms
Understanding Your Results: Clear Guidance Every Step
We understand that genetic test results can feel overwhelming. That’s why our process includes comprehensive genetic counselling to help you understand what your results mean for your family. Our expert team will walk you through:
- What specific genetic variations were found
- How these variations affect your child’s health
- Treatment and management recommendations
- Family implications and inheritance patterns
- Next steps for your child’s care journey
You’ll never be left wondering what your results mean or what to do next.
Transparent Pricing – Exceptional Value for South African Families
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| PIGN Syndrome NGS Genetic DNA Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | Included at no extra cost | ||
| Family Pedigree Analysis | Included at no extra cost | ||
Turnaround Time: 3-4 weeks | Sample Type: Blood, Extracted DNA, or Blood on FTA Card
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing across South Africa, including Johannesburg, Cape Town, Durban, and Pretoria
- Expert Genetic Team: Specialised paediatric geneticists and counsellors
- Advanced NGS Technology: State-of-the-art genetic sequencing for maximum accuracy
- Comprehensive Support: From sample collection to results interpretation
- Proven Track Record: Trusted by healthcare providers nationwide
Take the First Step Toward Understanding Your Child’s Health
Don’t let uncertainty about your child’s condition continue. Every day without answers is a day without the right interventions. Our PIGN Syndrome test provides the genetic clarity that can transform your child’s care journey.
Limited Time Offer: Special pricing of ZAR 6,700 available for a limited period. Secure your family’s genetic answers today.
Nationwide Access for All South Africans
We believe every South African family deserves access to quality genetic testing. Our services are available throughout the country, with convenient sample collection points in major cities and partnerships with local healthcare providers in regional areas.
