Understanding Your Child’s Seizures: A Compassionate Approach to Genetic Testing
Watching your infant experience seizures can be one of the most frightening experiences for any parent. The uncertainty, the worry, and the desperate need for answers can feel overwhelming. At Oracle Genomics, we understand the emotional journey you’re facing, and we’re here to provide the clarity and guidance you need through our comprehensive Dravet Syndrome and Early Infantile Epileptic Encephalopathy genetic test.
What This Test Detects: Gaining Clarity for Your Child’s Health
Our advanced Next Generation Sequencing test analyses 16 critical genes associated with severe epilepsy conditions in infants, including:
- SCN1A, SCN2A, SCN8A, SCN9A (sodium channel genes)
- GABRG2 (GABA receptor gene)
- KCNQ2, KCNT1 (potassium channel genes)
- CDKL5, ARX, STXBP1, and other crucial epilepsy-related genes
These genetic insights help identify the specific cause of your child’s seizures, enabling targeted treatment approaches that can significantly improve their quality of life.
Who Should Consider This Test: Recognizing the Signs
This test is particularly important if your infant shows:
- Frequent seizures that began in the first year of life
- Developmental delays or regression following seizure onset
- Seizures triggered by fever or temperature changes
- Resistance to standard anti-epileptic medications
- Family history of epilepsy or developmental disorders
- Abnormal movements, staring spells, or loss of consciousness
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Why Early Genetic Diagnosis Matters for Your Child’s Future
Receiving an accurate genetic diagnosis can transform your child’s healthcare journey by:
- Enabling targeted treatment strategies that work specifically for their genetic condition
- Helping avoid medications that might worsen their specific type of epilepsy
- Providing clarity about prognosis and expected developmental trajectory
- Opening doors to specialised support services and early intervention programmes
- Offering peace of mind through understanding the underlying cause
- Supporting family planning decisions with genetic counselling
Understanding Your Results: Clear Guidance Every Step of the Way
When your results are ready (within 40 working days), our team provides comprehensive explanations that help you understand:
- The specific genetic variant identified and its clinical significance
- How this finding relates to your child’s symptoms and treatment options
- Next steps for medical management and specialist referrals
- Resources and support networks available for your family
- Genetic counselling options for family members
Transparent Pricing and Value
| Service | Regular Price | Special Price |
|---|---|---|
| Dravet Syndrome Genetic Test | ZAR 8,700 | ZAR 7,800 |
| Turnaround Time | 40 Working Days | |
| Sample Collection | Daily by 9am at nationwide locations | |
Nationwide Accessibility and Trust
Oracle Genomics provides comprehensive genetic testing services across South Africa, with convenient sample collection points in Johannesburg, Cape Town, Durban, Pretoria, and major centres nationwide. Our partnership with leading neurologists ensures your child receives the expert care they deserve.
Take the First Step Toward Answers
Don’t let uncertainty about your child’s seizures continue to cause anxiety. Our genetic test provides the clarity needed to make informed decisions about their care. With our special pricing of ZAR 7,800 and nationwide accessibility, getting answers has never been more accessible.
Book your test today and take the first step toward understanding your child’s condition and accessing the right treatment path. Our compassionate team is ready to support you through this journey.
Note: This test requires a duly filled Whole Exome Sequencing Consent Form (Form 37) and 10mL whole blood sample collected in Lavender Top EDTA tubes.
