KCNQ3 Gene Seizures Benign Neonatal Type 2 NGS Genetic DNA Test
Comprehensive Genetic Testing for Neonatal Seizure Disorders
The KCNQ3 Gene Seizures Benign Neonatal Type 2 NGS Genetic DNA Test represents a breakthrough in pediatric neurological genetic diagnostics. This advanced test specifically targets mutations in the KCNQ3 gene, which plays a critical role in potassium channel function and neuronal excitability regulation. Benign familial neonatal seizures type 2 is an autosomal dominant inherited condition characterized by brief seizures occurring in otherwise healthy newborns during the first days to weeks of life.
What This Test Measures and Detects
Our comprehensive NGS-based genetic analysis examines the entire coding region of the KCNQ3 gene to identify:
- Point mutations affecting potassium channel function
- Missense mutations disrupting neuronal membrane stability
- Frameshift mutations altering protein structure
- Copy number variations affecting gene dosage
- Specific variants associated with benign neonatal seizure type 2
Who Should Consider This Genetic Test
This specialized genetic testing is recommended for:
- Newborns experiencing unexplained seizures within the first month of life
- Infants with family history of neonatal seizure disorders
- Patients with suspected benign familial neonatal epilepsy
- Individuals with recurrent seizures despite normal development
- Families seeking genetic counseling for inheritance patterns
Clinical Symptoms and Indications
Common clinical presentations that warrant KCNQ3 genetic testing include:
- Brief, recurrent seizures in otherwise healthy newborns
- Seizures typically lasting 1-2 minutes
- Normal interictal neurological examination
- Family history of similar neonatal seizure patterns
- Absence of metabolic or structural brain abnormalities
Benefits of KCNQ3 Genetic Testing
Undergoing this specialized genetic analysis provides numerous advantages for patients and families:
- Accurate Diagnosis: Differentiate between benign familial conditions and more serious neurological disorders
- Treatment Guidance: Inform appropriate anti-epileptic medication selection
- Genetic Counseling: Provide accurate recurrence risk information for family planning
- Prognostic Information: Understand the typically favorable long-term outcome
- Early Intervention: Enable timely management and monitoring strategies
Understanding Your Test Results
Our comprehensive genetic counseling services help you interpret your KCNQ3 test results:
- Positive Result: Indicates presence of a pathogenic KCNQ3 mutation, confirming diagnosis of benign familial neonatal seizures type 2
- Negative Result: Suggests absence of detectable KCNQ3 mutations, though other genetic causes should be considered
- Variant of Uncertain Significance: Identifies genetic changes with unclear clinical implications requiring further evaluation
- Carrier Status: Determines inheritance patterns for family members
Test Pricing and Details
| Test Component | Details |
|---|---|
| Test Name | KCNQ3 Gene Seizures Benign Neonatal 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 |
Pre-Test Requirements
Before scheduling your KCNQ3 genetic test, we require:
- Complete clinical history of the patient
- Genetic counseling session with our specialists
- Detailed pedigree chart of family members affected with similar conditions
- Neurological evaluation documentation
Nationwide Testing Availability
We provide comprehensive KCNQ3 genetic testing services across the United States with convenient locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, and many more. Our network of certified genetic counselors and neurologists ensures you receive expert care regardless of your location.
Book Your Genetic Test Today
Take the first step toward understanding your genetic health. Our team of genetic specialists is ready to guide you through the testing process and provide comprehensive result interpretation. Contact us today to schedule your appointment and begin your journey to genetic clarity.
Call or WhatsApp: +1(267) 388-9828
Don’t wait to get the answers you need about neonatal seizure disorders. Our advanced NGS technology and expert genetic counseling provide the comprehensive analysis required for accurate diagnosis and informed treatment decisions.
