Understanding Craniofrontonasal Syndrome: Your Path to Genetic Clarity
When you’re concerned about craniofrontonasal syndrome in your family, the uncertainty can feel overwhelming. We understand the emotional weight of genetic health questions and the need for clear, reliable answers. Our EFNB1 Gene NGS Genetic DNA Test is designed to provide the certainty you deserve, helping you make informed decisions about your family’s health journey.
What This Test Reveals About Your Genetic Health
The EFNB1 gene plays a crucial role in early development, particularly in the formation of facial features and skeletal structure. When mutations occur in this gene, it can lead to craniofrontonasal syndrome – a condition that affects skull and facial development. Our advanced Next Generation Sequencing (NGS) technology examines your EFNB1 gene with precision, identifying even the smallest genetic variations that could impact health outcomes.
Unlike basic genetic screens, our comprehensive analysis provides detailed information about specific mutations, giving you and your healthcare provider the complete picture needed for proper management and care planning.
Who Should Consider EFNB1 Genetic Testing?
This test is particularly important for families experiencing:
- Children with unusual facial features or skull development concerns
- Family history of craniofrontonasal syndrome or similar conditions
- Unexplained developmental delays in early childhood
- Planning for future pregnancies when genetic risks are a concern
- Individuals with diagnosed craniofrontonasal syndrome seeking confirmation
If you’ve noticed unusual facial characteristics, wide-set eyes, or skull shape concerns in your child, genetic testing can provide the answers that help guide appropriate medical care and support.
Why Early Genetic Detection Matters for Your Family
Understanding your genetic profile early can transform your family’s health journey. With EFNB1 testing, you gain:
- Peace of mind through definitive answers about genetic risks
- Informed family planning decisions based on accurate genetic information
- Early intervention opportunities for better developmental outcomes
- Personalised care planning with your healthcare team
- Reduced anxiety by replacing uncertainty with knowledge
Many families find that genetic testing provides the clarity needed to move forward with confidence, whether for current health management or future family planning.
Understanding Your Test Results with Compassion
We know that waiting for genetic test results can be an anxious time. That’s why we provide comprehensive support throughout the process:
- Clear, understandable reports written in patient-friendly language
- Included genetic counselling session to help interpret your results
- Direct connection to specialists if further care is needed
- Ongoing support for questions that arise after receiving results
Your genetic counsellor will help you understand what your results mean for your family’s health and connect you with appropriate resources and specialists.
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| EFNB1 Gene NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | INCLUDED at no extra cost | ||
| Family Pedigree Analysis | INCLUDED with your test | ||
Consider the long-term value: Early genetic detection can help avoid costly diagnostic odysseys and provide targeted care that improves quality of life.
Why South African Families Trust Oracle Genomics
Nationwide Accessibility
Convenient testing available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria. Multiple sample collection options to suit your needs.
Medical Expertise
Our team includes genetic specialists with extensive experience in pediatric genetic conditions, ensuring accurate analysis and compassionate care.
Advanced Technology
Using cutting-edge NGS technology for the most reliable genetic analysis available, with 99.9% accuracy in mutation detection.
Complete Support
From initial consultation through to results explanation, we provide comprehensive support every step of the way.
Test Information at a Glance
- Test Method: Next Generation Sequencing (NGS) Technology
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card
- Preparation Required: Clinical History and Genetic Counselling Session
- Medical Specialty: Pediatrics
Take the First Step Toward Genetic Clarity Today
Don’t let uncertainty about genetic health concerns weigh on your family. With our special pricing of ZAR 6,700 (saving you ZAR 2,650), now is the perfect time to get the answers you need.
Urgent Note: Early genetic detection can significantly impact developmental outcomes and family planning decisions. Don’t delay in getting the information that could transform your family’s health journey.
