Understanding Duchenne and Becker Muscular Dystrophy Genetic Testing
When you notice your child struggling with muscle weakness, delayed motor skills, or difficulty keeping up with peers, the worry can be overwhelming. Our Duchenne Becker Muscular Dystrophy (DMD BMD) Gene Mutation Test provides the answers you need to navigate these concerns with confidence and clarity.
What This Test Detects
This advanced genetic screening identifies mutations in the dystrophin gene responsible for both Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD). Using sophisticated MLPA (Multiplex Ligation-dependent Probe Amplification) technology, we examine specific gene deletions and duplications that cause these progressive muscle disorders. Understanding your genetic profile empowers you to make informed healthcare decisions for your family.
Who Should Consider This Test
This test is particularly important if you or your child experience:
- Progressive muscle weakness starting in early childhood
- Delayed motor milestones (walking, running, climbing)
- Frequent falls or difficulty rising from sitting position
- Enlarged calf muscles (pseudohypertrophy)
- Family history of muscular dystrophy
- Elevated creatine kinase levels in blood tests
Why Early Detection Matters for Your Health
Early genetic identification of DMD/BMD provides crucial benefits:
- Timely Intervention: Access to appropriate treatments and therapies sooner
- Family Planning: Informed reproductive decisions for future generations
- Peace of Mind: Reduced uncertainty about your child’s health journey
- Specialist Referral: Direct connection to pediatric neurologists and muscle specialists
- Support Networks: Early access to muscular dystrophy support communities
Understanding Your Results
Our genetic counselors provide clear, compassionate explanations of your results. Whether the test identifies a mutation or returns normal findings, you’ll receive comprehensive guidance on next steps. Positive results connect you with specialist care, while negative results provide valuable reassurance about your family’s genetic health.
Transparent Pricing – Exceptional Value
| Test Option | Price | Savings |
|---|---|---|
| Regular Price | ZAR 6,000 | – |
| Special Offer | ZAR 4,700 | ZAR 1,300 |
This investment in your family’s health provides lifelong value through early detection and intervention opportunities.
Nationwide Accessibility
We serve patients across South Africa with convenient testing locations in Johannesburg, Cape Town, Durban, Pretoria, and surrounding areas. Our network ensures you receive the same high-quality genetic testing regardless of your location.
Trust Our Expertise
Oracle Genomics partners with leading physicians, pediatricians, and neurologists to deliver medically accurate genetic testing. Our MLPA methodology ensures 99.9% accuracy, and our 3-week turnaround time respects your need for timely answers.
Take Action Today
Don’t let uncertainty about muscular dystrophy create unnecessary anxiety. Our simple blood test requires only a duly filled Genomics Clinical Information Requisition Form (Form 20) to begin your genetic health journey.
Book your DMD BMD Gene Mutation Test today and take the first step toward genetic clarity and peace of mind.
Contact us now to schedule your test at one of our nationwide locations or speak with our genetic counseling team about your specific concerns.
