WWOX Gene Early Infantile Epileptic Encephalopathy Type 28 NGS Genetic DNA Test

Understanding Your Baby’s Neurological Health: The WWOX Gene Epilepsy Test

As parents, nothing matters more than your baby’s health and development. When seizures or developmental concerns arise in infancy, the uncertainty can be overwhelming. Our WWOX Gene Early Infantile Epileptic Encephalopathy Type 28 test provides the clarity and answers you need during this challenging time. This specialised genetic test focuses on detecting mutations that cause severe epilepsy syndromes appearing in the first months of life.

What This Test Detects

This advanced Next-Generation Sequencing (NGS) test specifically examines the WWOX gene for mutations responsible for Early Infantile Epileptic Encephalopathy Type 28. This rare genetic condition typically manifests in the first 3-6 months of life with difficult-to-control seizures, developmental regression, and significant neurological challenges. By identifying the specific genetic cause, we can help guide appropriate treatment strategies and provide accurate prognosis information.

Who Should Consider This Test

This test is particularly important for families where:

• Your infant experiences frequent, difficult-to-control seizures starting in early infancy
• There’s developmental regression or delayed milestones following seizure onset
• Your baby shows abnormal brain activity patterns on EEG testing
• There’s a family history of infantile epilepsy or unexplained infant deaths
• Previous epilepsy treatments have shown limited effectiveness
• You’re planning another pregnancy and want to understand genetic risks

Why Early Detection Matters for Your Family

Identifying WWOX gene mutations early provides several crucial benefits:

• Targeted Treatment Planning: Knowing the specific genetic cause helps neurologists develop more effective treatment strategies
• Developmental Support: Early intervention can help maximise your child’s developmental potential
• Family Planning Guidance: Understand recurrence risks for future pregnancies
• Peace of Mind: Replace uncertainty with clear answers and a defined path forward
• Medical Management: Guide appropriate medication choices and avoid ineffective treatments

Understanding Your Results

Our comprehensive genetic counselling service ensures you fully understand your test results and their implications. We provide:

• Clear explanation of genetic findings in understandable language
• Discussion of what the results mean for your child’s care and development
• Guidance on next steps and specialist referrals if needed
• Family pedigree analysis to understand inheritance patterns
• Ongoing support for questions that may arise after receiving results

Investment in Your Child’s Health

Nationwide Trust and Accessibility

Oracle Genomics brings advanced genetic testing to families across South Africa. With convenient testing locations in Johannesburg, Cape Town, Durban, and Pretoria, we ensure that every family has access to the genetic answers they need. Our partnership with leading neurologists and genetic specialists guarantees the highest standard of care and interpretation.

Take the Next Step Toward Answers

Don’t let uncertainty about your baby’s neurological health create unnecessary stress. Early genetic testing can provide the clarity needed to make informed decisions about your child’s care. Our compassionate team understands the emotional journey you’re on and is here to support you every step of the way.

Trust Oracle Genomics for accurate, compassionate genetic care. Your family’s neurological health deserves the clarity that advanced genetic testing provides.