Understanding MED12 Lujan-Fryns Syndrome: Your Family’s Genetic Health Matters
When you notice developmental delays or intellectual challenges in your child, it’s natural to feel concerned and seek answers. The MED12 Gene Lujan-Fryns Syndrome NGS Genetic DNA Test provides the clarity you need to understand your family’s genetic health and plan for the future with confidence.
What This Test Detects
The MED12 gene plays a crucial role in normal development and intellectual function. Our advanced Next-Generation Sequencing (NGS) technology examines this gene for mutations that can cause Lujan-Fryns syndrome – a condition characterized by intellectual disability, distinctive facial features, and behavioural challenges.
By identifying these genetic changes early, you can access targeted interventions and support that can significantly improve quality of life and developmental outcomes.
Who Should Consider This Test?
This test is particularly important if your child or family member shows:
- Unexplained developmental delays or intellectual disability
- Distinctive facial features (long face, high forehead, small jaw)
- Behavioural challenges or autism spectrum characteristics
- Family history of similar symptoms across generations
- Marfanoid body habitus (tall, slender build)
Early genetic testing can provide answers that help guide educational support, behavioural therapy, and medical management.
Why Early Detection Matters for Your Family
Getting a definitive diagnosis through genetic testing offers multiple benefits:
- Personalized Care Planning: Understand exactly what support and interventions will be most effective
- Family Planning Guidance: Make informed decisions about future pregnancies with genetic counselling
- Reduced Diagnostic Uncertainty: End the cycle of doctor visits and unanswered questions
- Access to Support Services: Connect with appropriate educational and therapeutic resources
- Peace of Mind: Finally understand the cause of developmental challenges
Understanding Your Results
Our comprehensive genetic counselling service ensures you fully understand your test results and their implications. We provide:
- Clear, easy-to-understand explanation of genetic findings
- Personalized guidance on next steps and management options
- Family pedigree analysis to understand inheritance patterns
- Connection to appropriate medical specialists and support networks
- Ongoing support for any questions that arise after testing
Remember: A genetic diagnosis doesn’t define your child – it empowers you to provide the best possible support.
Transparent Pricing – Investing in Your Family’s Future
| Service | Regular Price | Special Price |
|---|---|---|
| MED12 Lujan-Fryns Syndrome NGS Test | ZAR 6,700 |
What’s Included: Comprehensive genetic analysis, genetic counselling session, family pedigree chart, detailed results report, and post-test support.
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Why Trust Oracle Genomics?
- Nationwide Coverage: Serving families across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Specialized in pediatric genetic conditions with South African context
- Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
- Comprehensive Support: Genetic counselling included with every test
- Proven Track Record: Trusted by South African families and healthcare providers
Take the First Step Toward Understanding
Don’t let uncertainty about your child’s development create unnecessary stress. Our MED12 Lujan-Fryns Syndrome test provides the answers you need to move forward with confidence.
Early detection leads to better outcomes. The sooner you understand the genetic factors at play, the sooner you can access appropriate support and interventions.
Ready to get answers? Contact Oracle Genomics today at [Phone Number] or book your genetic counselling session online. Your family’s health journey starts with understanding.
Limited time special pricing of ZAR 6,700 available. Regular price ZAR 9,350.
