Understanding Your Infant’s Neurological Health: The PLCB1 Gene Test
When your infant shows signs of developmental delays or unusual movements, the uncertainty can be overwhelming. As parents in South Africa, you deserve clear answers and a path forward. The PLCB1 Gene Early Infantile Epileptic Encephalopathy Type 12 test provides that clarity through advanced genetic technology that identifies the root cause of severe epilepsy conditions.
What This Test Reveals About Your Child’s Health
The PLCB1 gene plays a critical role in brain development and function. When mutations occur in this gene, they can lead to Early Infantile Epileptic Encephalopathy Type 12 – a severe form of epilepsy that typically appears in the first months of life. Our Next-Generation Sequencing (NGS) technology examines this gene with exceptional precision, identifying even the smallest genetic variations that could be affecting your child’s neurological health.
Is This Test Right for Your Family?
This test is particularly important if your infant shows:
- Early-onset seizures (before 3 months of age)
- Developmental regression or delays
- Abnormal muscle tone or movements
- Family history of infantile epilepsy
- Unexplained neurological symptoms
Many South African families in Johannesburg, Cape Town, and Durban have found answers through this testing, enabling earlier interventions and better management strategies.
Why Early Detection Matters for Your Child’s Future
Early diagnosis through PLCB1 gene testing can significantly impact your child’s quality of life by:
- Enabling targeted treatment approaches
- Providing accurate prognosis information
- Reducing diagnostic uncertainty and stress
- Informing family planning decisions
- Connecting you with appropriate support services
The peace of mind that comes with a definitive diagnosis is invaluable for South African families navigating complex neurological conditions.
Understanding Your Test Results
Our comprehensive results package includes:
- Clear, easy-to-understand report explaining the genetic findings
- Professional interpretation by our neurological genetics specialists
- Genetic counselling session to discuss implications
- Recommendations for next steps and management
- Connection to appropriate medical specialists if needed
We ensure you never feel alone in understanding your results, with ongoing support available throughout your journey.
Transparent Pricing for South African Families
| Service | Regular Price | Special Price |
|---|---|---|
| PLCB1 Gene Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling | Included | |
| Results Interpretation | Included | |
| Turnaround Time | 3-4 Weeks | |
This investment in your child’s health can save thousands in unnecessary treatments and provide clarity that lasts a lifetime.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing from Johannesburg to Cape Town, Durban to Pretoria
- Medical Expertise: Collaboration with leading neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS testing with 99.9% accuracy
- Compassionate Care: Understanding the emotional journey of genetic testing
- Proven Results: Helping hundreds of South African families find answers
Take the First Step Toward Answers Today
Don’t let uncertainty about your infant’s health create unnecessary stress. Early detection through PLCB1 gene testing can provide the clarity you need to make informed decisions about your child’s care.
Limited Time Special: Book now to secure the ZAR 6,700 price and take control of your child’s neurological health journey. Our team is ready to support you every step of the way.
