Understanding Your Child’s Neurological Health
As a parent, watching your infant experience seizures or developmental challenges can be overwhelming and frightening. We understand the deep concern you feel when your child’s health is at stake. Our DNM1 Gene Early Infantile Epileptic Encephalopathy Type 31 NGS Genetic DNA Test is designed to provide the answers you desperately need, offering clarity and direction for your child’s medical care.
What This Test Detects
This advanced genetic test specifically examines the DNM1 gene for mutations that cause Early Infantile Epileptic Encephalopathy Type 31 (EIEE31). DNM1 plays a crucial role in brain function, particularly in neurotransmitter release at nerve cell connections. When mutations occur, they disrupt normal brain activity, leading to severe epilepsy that typically begins in the first months of life.
Who Should Consider This Test
This test is essential for infants and young children experiencing:
- Frequent seizures or epileptic spasms starting in early infancy
- Developmental regression or delayed milestones
- Abnormal EEG patterns suggestive of epileptic encephalopathy
- Family history of early-onset epilepsy or neurological disorders
- Unexplained developmental delays with seizure activity
Why Early Detection Matters for Your Child’s Future
Identifying DNM1 mutations early can significantly impact your child’s treatment outcomes and quality of life. Accurate diagnosis allows for:
- Targeted treatment strategies specific to DNM1-related epilepsy
- Better seizure control through appropriate medication selection
- Early intervention services to support development
- Family planning guidance and genetic counselling for future pregnancies
- Connection to specialist care and support networks
Understanding Your Results with Compassion
We know receiving genetic test results can be emotionally challenging. Our team provides comprehensive support throughout the process:
- Clear, easy-to-understand result explanations
- Genetic counselling to discuss implications and next steps
- Connection to paediatric neurologists and epilepsy specialists
- Ongoing support for treatment planning and management
- Privacy and confidentiality guaranteed throughout
Affordable, Accessible Testing for South African Families
| Service | Regular Price | Special Price |
|---|---|---|
| DNM1 Genetic Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Result Interpretation | Included | |
Trusted Nationwide Coverage
We serve families across South Africa with convenient testing locations in Johannesburg, Cape Town, Durban, Pretoria, and nationwide. Our network of qualified healthcare professionals ensures you receive the same high standard of care regardless of your location.
Take the First Step Toward Answers
Don’t let uncertainty about your child’s health create unnecessary stress. Early detection through genetic testing can provide the clarity needed for effective treatment and improved outcomes. Our compassionate team is ready to support your family through this journey.
Book your consultation today and take the first step toward understanding your child’s neurological health. With results in 3-4 weeks and comprehensive support throughout the process, we’re here to help you navigate this challenging time with confidence and care.
