Find Clarity for Your Child’s Neurological Health
When your child faces developmental challenges or shows signs of muscle weakness, the uncertainty can be overwhelming. Our B4GAT1 Gene Muscular Dystrophy-Dystroglycanopathy Type A13 NGS Genetic DNA Test provides the answers you need to make informed decisions about your child’s care and future.
Understanding the B4GAT1 Genetic Test
This specialised genetic test examines the B4GAT1 gene for mutations that cause a rare but serious form of congenital muscular dystrophy. When this gene doesn’t function properly, it affects how muscles, brain tissue, and eye structures develop, leading to the characteristic symptoms of Type A13 dystroglycanopathy.
Using Next-Generation Sequencing (NGS) technology, we analyse your DNA with exceptional precision, identifying even the smallest genetic variations that could impact your child’s health.
Who Should Consider This Genetic Test?
This test is particularly important if your child shows:
- Severe muscle weakness from birth or early infancy
- Delayed motor development milestones
- Brain abnormalities detected on MRI scans
- Eye structure anomalies or vision problems
- Family history of similar neurological conditions
- Unexplained developmental delays with muscle involvement
If you’re planning a pregnancy and have family members affected by similar conditions, genetic counselling and testing can provide valuable insights for family planning decisions.
Why Early Detection Matters for Your Child’s Future
Getting a definitive diagnosis through genetic testing offers multiple benefits:
- Accurate Diagnosis: Move beyond uncertainty to a clear understanding of your child’s condition
- Personalised Care: Enable healthcare providers to create targeted treatment plans
- Family Planning: Understand inheritance patterns for future family decisions
- Early Intervention: Access appropriate therapies and support services sooner
- Peace of Mind: Reduce the stress of not knowing and focus on effective management
Understanding Your Test Results
Our genetic counsellors will walk you through your results with compassion and clarity:
- Positive Result: Confirms the presence of B4GAT1 gene mutations. Our team will connect you with specialists and support resources
- Negative Result: Rules out this specific form of muscular dystrophy, helping direct further medical investigation
- Variant of Uncertain Significance: Identifies a genetic change whose impact isn’t fully understood, with guidance on monitoring and follow-up
Regardless of the outcome, you’ll receive comprehensive support and next-step recommendations.
Transparent Pricing & Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| B4GAT1 Gene Test | ZAR 6,700 | ZAR 2,650 |
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or Blood on FTA Card
This investment in your child’s health can save thousands in unnecessary medical tests and provide direction for effective care management.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS technology for 99.9% accuracy
- Comprehensive Support: Genetic counselling included with every test
- Confidential Service: Your privacy and data security are our top priorities
Take the First Step Toward Clarity Today
Don’t let uncertainty about your child’s health create unnecessary stress. Our compassionate team is ready to guide you through the genetic testing process with expertise and understanding.
Limited Time Offer: Special pricing of ZAR 6,700 available for immediate bookings. Early detection can make a significant difference in managing your child’s condition effectively.
