Understanding Your Child’s Development: AP4M1 Gene Microcephaly Testing
As a parent, noticing developmental concerns in your child can be overwhelming. When microcephaly (small head size) or motor development delays appear, it’s natural to seek clear answers. Our AP4M1 Gene Microcephaly NGS Genetic DNA Test provides the definitive genetic information you need to understand your child’s condition and plan for their future with confidence.
What This Test Detects
The AP4M1 gene plays a crucial role in brain development and nerve function. Mutations in this gene can cause hereditary spastic paraplegia type 50 (SPG50), characterized by microcephaly, developmental delays, and progressive muscle stiffness. Our advanced Next Generation Sequencing (NGS) technology examines the AP4M1 gene with exceptional accuracy, identifying even subtle genetic variations that might be missed by conventional testing methods.
Who Should Consider This Test
This test is particularly important if your child shows:
- Microcephaly (smaller than average head circumference)
- Delayed motor development milestones
- Progressive leg stiffness or walking difficulties
- Intellectual disability or learning challenges
- Family history of similar neurological conditions
Early genetic diagnosis can guide appropriate interventions and help manage expectations for your child’s development.
Why Early Genetic Diagnosis Matters
Receiving a definitive genetic diagnosis provides multiple benefits for your family’s health journey:
- Clarity and Peace of Mind: End the uncertainty about your child’s condition
- Personalized Care Planning: Guide therapy and educational interventions
- Family Planning Insights: Understand inheritance risks for future pregnancies
- Early Intervention Opportunities: Access appropriate support services sooner
- Medical Management Guidance: Work with specialists on targeted treatment approaches
Understanding Your Results
We know waiting for genetic test results can be stressful. Our comprehensive report includes:
- Clear explanation of any AP4M1 gene mutations detected
- Interpretation of what the results mean for your child’s health
- Information about inheritance patterns and family implications
- Recommendations for next steps and specialist consultations
- Access to our genetic counselling team for result discussion
Our team ensures you fully understand the results and their implications for your family.
Transparent Pricing & Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| AP4M1 Gene Microcephaly NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | Included at no extra cost | ||
| Family Pedigree Analysis | Included at no extra cost | ||
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Why Trust Oracle Genomics
As South Africa’s leading genetic testing provider, we combine medical excellence with compassionate care:
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Advanced Technology: Next Generation Sequencing for highest accuracy
- Expert Genetic Counselling: Professional guidance included with every test
- Pediatric Specialization: Experience in children’s genetic conditions
- Confidential & Secure: Your family’s privacy is our priority
Take the First Step Toward Clarity
Don’t let uncertainty about your child’s development continue. Our AP4M1 Gene Microcephaly test provides the answers you need to make informed decisions about your child’s care and future.
Limited Time Offer: Save ZAR 2,650 on comprehensive AP4M1 testing with included genetic counselling. Take action today for your child’s healthier tomorrow.
