Understanding Your Child’s Brain Development: SEPSECS Gene Testing for Pontocerebellar Hypoplasia
We understand the deep concern that comes when your child shows signs of developmental delays or neurological symptoms. The uncertainty can be overwhelming, but you don’t have to face it alone. Our SEPSECS Gene Pontocerebellar Hypoplasia Type 2D NGS Genetic DNA Test provides the clarity and answers your family needs to move forward with confidence.
What This Test Reveals About Your Child’s Health
This advanced genetic test specifically examines the SEPSECS gene for mutations that can cause Pontocerebellar Hypoplasia Type 2D (PCH2D). This rare neurological disorder affects brain development, particularly in the cerebellum and pons areas that control movement, coordination, and other essential functions. Using Next-Generation Sequencing (NGS) technology, we provide the most accurate analysis available.
When Should You Consider This Genetic Test?
This test is particularly important if your child shows:
- Developmental delays in motor skills and coordination
- Progressive microcephaly (small head size)
- Muscle weakness or poor muscle tone
- Difficulty with balance and walking
- Speech and language development concerns
- Family history of similar neurological conditions
Early detection can make a significant difference in managing symptoms and planning appropriate interventions.
Why Early Detection Matters for Your Family
Getting clear answers through genetic testing provides multiple benefits:
- Peace of Mind: Eliminate uncertainty and get definitive answers
- Informed Decisions: Guide treatment and therapy choices based on accurate diagnosis
- Family Planning: Understand genetic risks for future pregnancies
- Early Intervention: Start appropriate therapies and support sooner
- Medical Management: Work with specialists to create the best care plan
Understanding Your Test Results
We know waiting for genetic test results can be stressful. Our team provides:
- Clear Explanations: Simple, understandable reports with expert interpretation
- Genetic Counselling: Professional guidance to help you understand the implications
- Follow-up Support: Connection to appropriate medical specialists
- Family Guidance: Information about what results mean for other family members
Our genetic counsellors are here to support you every step of the way.
Affordable Genetic Testing for South African Families
| Test Option | Price | Turnaround Time |
|---|---|---|
| SEPSECS PCH2D NGS Genetic Test | ZAR 6,700 (Regular ZAR 9,350) | 3-4 Weeks |
What’s Included: Comprehensive genetic analysis, professional genetic counselling session, detailed results report, and ongoing support.
Sample Collection: Simple blood draw or blood spot on FTA card – available at our nationwide collection centres.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Convenient testing available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: Latest NGS technology for maximum accuracy
- Professional Support: Genetic counselling included with every test
- Proven Reliability: Trusted by healthcare professionals nationwide
Take the First Step Toward Clarity Today
Don’t let uncertainty about your child’s neurological health create unnecessary stress. Our genetic testing provides the answers you need to make informed decisions about their care and future.
Early detection leads to better outcomes. The sooner you have answers, the sooner you can take appropriate action for your child’s health and development.
