Find Answers for Your Infant’s Neurological Health
When your infant experiences unexplained seizures or developmental delays, the uncertainty can be overwhelming. Our KCNB1 Gene Early Infantile Epileptic Encephalopathy Type 26 NGS Genetic DNA Test provides the clarity South African families need to understand their child’s condition and make informed healthcare decisions.
Understanding the KCNB1 Gene Test
This specialised genetic test examines the KCNB1 gene using advanced Next-Generation Sequencing (NGS) technology. The KCNB1 gene plays a crucial role in brain function, and mutations in this gene can lead to Early Infantile Epileptic Encephalopathy Type 26 – a severe form of epilepsy that typically appears in the first months of life.
Our test provides comprehensive analysis of this specific gene, helping to identify the genetic cause behind neurological symptoms and guiding appropriate treatment strategies for your child.
Who Should Consider This Test?
This test is particularly important for infants and young children experiencing:
- Unexplained seizures or epilepsy that began in early infancy
- Developmental delays or regression in motor skills
- Abnormal brain activity detected through EEG testing
- Family history of similar neurological conditions
- Resistance to standard anti-epileptic medications
If your child has been diagnosed with epileptic encephalopathy or shows concerning neurological symptoms, this test can provide essential genetic information.
Why This Test Matters for Your Child’s Health
Early genetic diagnosis through our KCNB1 test offers multiple benefits:
- Accurate Diagnosis: Confirm whether KCNB1 mutations are causing your child’s symptoms
- Personalised Treatment: Guide medication choices and management strategies
- Family Planning: Understand inheritance patterns for future family planning
- Prognostic Information: Gain insights into potential developmental outcomes
- Peace of Mind: Reduce uncertainty and make informed healthcare decisions
Understanding Your Test Results
Our comprehensive genetic counselling service ensures you fully understand your results. We provide:
- Clear explanation of genetic findings in simple, understandable language
- Discussion of what the results mean for your child’s treatment and development
- Guidance on next steps and available support resources
- Family pedigree analysis to understand inheritance patterns
- Ongoing support from our neurological genetics specialists
Remember: A positive result provides valuable information for managing your child’s condition, while a negative result helps rule out this specific cause, directing attention to other potential factors.
Affordable Genetic Testing for South African Families
| Test Feature | Details | Value |
|---|---|---|
| Regular Price | ZAR 9,350 | Comprehensive genetic analysis |
| Special Price | ZAR 6,700 | Save ZAR 2,650 |
| Turnaround Time | 3-4 Weeks | Timely results for urgent decisions |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card | Convenient collection options |
Consider the long-term value: Early diagnosis can prevent unnecessary treatments and guide effective management strategies, potentially saving significant healthcare costs over time.
Why Trust Oracle Genomics?
We understand the sensitivity of genetic testing for neurological conditions in children. Our approach combines:
- Medical Expertise: Collaboration with neurologists and genetic specialists
- Advanced Technology: NGS technology for highest accuracy
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Genetic Counselling: Comprehensive pre- and post-test support
- Patient-Centred Care: Empathetic approach to sensitive family situations
Take the First Step Toward Understanding
Don’t let uncertainty about your child’s neurological health continue. Our KCNB1 gene test provides the answers you need to move forward with confidence.
What’s Included:
- Comprehensive KCNB1 gene analysis using NGS technology
- Genetic counselling session with family pedigree analysis
- Clear, detailed results report with clinical interpretation
- Ongoing support from our neurological genetics team
- Convenient sample collection options nationwide
Early detection through genetic testing can make a significant difference in managing neurological conditions. Contact us today to schedule your genetic counselling session and take the first step toward understanding your child’s health.
