PRRT2 Gene Seizures Benign Familial Infantile Type 2 NGS Genetic DNA Test
Comprehensive Introduction to PRRT2 Genetic Testing
The PRRT2 Gene Seizures Benign Familial Infantile Type 2 NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying genetic mutations associated with benign familial infantile seizures. This neurological condition, characterized by recurrent seizures in infancy with a strong genetic component, requires precise genetic analysis for accurate diagnosis and management. Our advanced next-generation sequencing technology provides comprehensive analysis of the PRRT2 gene, offering families crucial insights into their genetic predisposition and enabling informed healthcare decisions.
What This Test Measures and Detects
This specialized genetic test focuses on identifying mutations within the PRRT2 (Proline-Rich Transmembrane Protein 2) gene, which plays a critical role in neurotransmitter release and neuronal communication. The test specifically detects:
- Point mutations and small insertions/deletions in the PRRT2 gene
- Genetic variants associated with benign familial infantile seizures type 2
- Inheritance patterns of seizure disorders within families
- Specific genetic markers that predispose individuals to infantile seizures
Who Should Consider This Genetic Test
This test is particularly recommended for individuals and families experiencing:
- Infants with recurrent seizures beginning between 3-12 months of age
- Families with multiple members affected by infantile seizures
- Individuals with a family history of benign familial infantile epilepsy
- Patients with seizure disorders that resolve spontaneously in early childhood
- Families planning pregnancy with known seizure disorders in their genetic history
Common Symptoms and Clinical Indications
- Recurrent focal seizures in infancy
- Seizures triggered by fever or infection
- Normal development between seizure episodes
- Family history of similar seizure patterns
- Seizures that typically resolve by age 2-3 years
Significant Benefits of PRRT2 Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous advantages for patients and families:
- Accurate Diagnosis: Confirms genetic basis of seizure disorders
- Family Planning: Enables informed reproductive decisions
- Treatment Guidance: Helps neurologists develop targeted treatment strategies
- Prognostic Information: Provides insights into disease progression and outcomes
- Genetic Counseling: Supports families in understanding inheritance patterns
- Early Intervention: Facilitates timely management of seizure episodes
Understanding Your Test Results
Our comprehensive genetic counseling services help you interpret your results effectively:
- Positive Result: Indicates presence of PRRT2 gene mutation associated with benign familial infantile seizures
- Negative Result: Suggests absence of tested mutations, though other genetic factors may be involved
- Variant of Uncertain Significance: Requires additional family studies and clinical correlation
- Carrier Status: Identifies individuals who may pass the condition to offspring
Post-Test Guidance
Following your results, our genetic specialists provide:
- Detailed explanation of genetic findings
- Discussion of inheritance patterns and recurrence risks
- Referrals to neurological specialists for ongoing care
- Family testing recommendations when appropriate
- Long-term monitoring and management strategies
Test Pricing and Details
| Test Feature | Details |
|---|---|
| Test Name | PRRT2 Gene Seizures Benign Familial Infantile Type 2 NGS Genetic DNA Test |
| Discount Price | $500 USD |
| Regular Price | $700 USD |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type | Blood, Extracted DNA, or One Drop Blood on FTA Card |
| Testing Method | Next-Generation Sequencing (NGS) Technology |
Nationwide Testing Availability
We proudly serve patients across the United States with convenient testing locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified genetic testing facilities ensures consistent, high-quality results regardless of your location.
Pre-Test Requirements and Preparation
To ensure optimal testing outcomes, we require:
- Complete clinical history of the patient undergoing testing
- Genetic counseling session to create detailed family pedigree chart
- Documentation of affected family members with seizure disorders
- Neurological evaluation and referral when appropriate
Take Control of Your Genetic Health Today
Don’t let uncertainty about genetic seizure disorders impact your family’s future. Our comprehensive PRRT2 genetic testing provides the clarity and confidence you need for informed healthcare decisions. With advanced NGS technology and expert genetic counseling, we deliver accurate, reliable results that can transform your approach to neurological health management.
Ready to schedule your test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online. Take the first step toward understanding your genetic health and securing your family’s neurological well-being.
