Find Answers for Your Child’s Brain Development Concerns
As a parent, watching your child struggle with developmental delays or seizures can be heartbreaking and overwhelming. You deserve clear answers and a path forward. Our RELN Gene Lissencephaly Type 2 NGS Genetic DNA Test provides the definitive diagnosis you need to understand your child’s condition and make informed healthcare decisions.
Understanding the RELN Gene Lissencephaly Test
Lissencephaly Type 2, also known as Norman-Roberts syndrome, is a rare genetic disorder that affects brain development. The condition is caused by mutations in the RELN gene, which plays a crucial role in guiding brain cell migration during fetal development. Our advanced Next-Generation Sequencing (NGS) technology examines the entire RELN gene to identify any mutations that could be causing your child’s symptoms.
This isn’t just another test – it’s a comprehensive genetic analysis that provides the clarity needed for proper diagnosis and management. Unlike basic genetic screens, our NGS approach offers unparalleled accuracy in detecting even the most subtle genetic variations.
Who Should Consider This Genetic Test?
This test is essential for families who have noticed:
- Significant developmental delays in their infant or young child
- Recurrent seizures or epilepsy that began in infancy
- Abnormal brain MRI scans showing smooth brain surface (lissencephaly)
- Family history of similar neurological conditions
- Unexplained muscle weakness or feeding difficulties in infancy
- Delayed motor milestones like sitting, crawling, or walking
If your child has been diagnosed with cerebral palsy but the cause remains unclear, this test can provide the genetic answers you’ve been searching for.
Why Early Genetic Diagnosis Matters for Your Child’s Future
Getting a definitive diagnosis through genetic testing transforms uncertainty into actionable information. With accurate genetic results, you can:
- Access targeted treatments and therapies specific to your child’s condition
- Make informed decisions about future family planning
- Connect with support groups and specialists who understand your child’s specific needs
- Develop a comprehensive care plan with your healthcare team
- Reduce the stress of diagnostic uncertainty and multiple medical appointments
- Understand the prognosis and what to expect as your child grows
Early diagnosis means earlier intervention – and that can make a significant difference in your child’s quality of life.
Understanding Your Test Results – Clear Guidance Every Step
We understand that waiting for genetic test results can be anxiety-provoking. That’s why we provide comprehensive support throughout the process:
- Pre-test Genetic Counselling: Before testing, you’ll meet with our genetic counsellor who will create a detailed family history and explain what to expect
- Clear Result Interpretation: Your results will be presented in easy-to-understand language with clear explanations
- Post-test Support: We help you understand what your results mean for your child’s care and future health
- Medical Team Coordination: We can coordinate with your child’s neurologist or pediatrician to ensure seamless care
Remember: A positive result provides answers and direction. A negative result can rule out this specific condition, helping your medical team focus on other potential causes.
Transparent Pricing – Exceptional Value for Peace of Mind
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| RELN Gene Lissencephaly Type 2 NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | Included at no extra cost | ||
| Result Interpretation | Included at no extra cost | ||
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Consider this: The cost of ongoing diagnostic uncertainty, multiple specialist visits, and delayed interventions often far exceeds the investment in this definitive genetic test.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing services across South Africa, including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Our team includes genetic specialists with extensive experience in pediatric neurological disorders
- Advanced Technology: We use cutting-edge NGS technology for the most accurate results available
- Patient-Centred Care: Every test includes comprehensive genetic counselling and support
- Proven Accuracy: Our testing methods meet international standards for genetic diagnosis
- Local Understanding: We understand the unique healthcare landscape and family needs in South Africa
Take the First Step Toward Answers Today
Don’t let uncertainty about your child’s condition continue to cause stress and worry. The answers you need are within reach.
Important: Early diagnosis leads to earlier interventions. Don’t delay getting the answers that could significantly impact your child’s developmental outcomes.
