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ST3GAL3 Gene Early Infantile Epileptic Encephalopathy Type 15 Genetic Test

Original price was: $700.Current price is: $500.

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The ST3GAL3 Gene Early Infantile Epileptic Encephalopathy Type 15 NGS Genetic DNA Test is a specialized diagnostic tool that identifies mutations in the ST3GAL3 gene responsible for severe neurological disorders in infants. This comprehensive next-generation sequencing test provides crucial genetic information for families affected by early-onset seizures and developmental delays. The test helps confirm diagnosis, guide treatment decisions, and provide valuable information for family planning. Available for $500 USD, this advanced genetic testing offers peace of mind through accurate detection of pathogenic variants associated with this rare epileptic encephalopathy condition.

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ST3GAL3 Gene Early Infantile Epileptic Encephalopathy Type 15 NGS Genetic DNA Test

Understanding ST3GAL3 Gene-Related Epileptic Encephalopathy

Early Infantile Epileptic Encephalopathy Type 15 is a rare but severe neurological disorder caused by mutations in the ST3GAL3 gene. This condition typically manifests in the first months of life and is characterized by treatment-resistant seizures, developmental regression, and significant neurological impairment. The ST3GAL3 gene plays a crucial role in brain development and function, particularly in the formation of complex brain structures and neural connectivity.

What Does This Test Measure?

Our advanced NGS Genetic DNA Test specifically targets the ST3GAL3 gene to identify pathogenic variants responsible for Early Infantile Epileptic Encephalopathy Type 15. The test utilizes next-generation sequencing technology to comprehensively analyze:

  • Point mutations and single nucleotide variants
  • Small insertions and deletions
  • Copy number variations affecting the ST3GAL3 gene
  • Regulatory region abnormalities

Who Should Consider This Test?

This genetic test is recommended for infants and children presenting with specific clinical symptoms including:

  • Early-onset seizures within the first 6 months of life
  • Developmental regression or stagnation
  • Abnormal EEG patterns consistent with epileptic encephalopathy
  • Family history of similar neurological conditions
  • Unexplained developmental delays with seizure activity
  • Resistance to conventional anti-epileptic medications

Clinical Benefits of ST3GAL3 Genetic Testing

Undergoing this specialized genetic test provides numerous advantages for patients and families:

  • Accurate Diagnosis: Confirms or rules out ST3GAL3-related epileptic encephalopathy
  • Treatment Guidance: Helps neurologists develop targeted treatment strategies
  • Prognostic Information: Provides insight into disease progression and outcomes
  • Family Planning: Enables genetic counseling for future pregnancies
  • Early Intervention: Facilitates timely therapeutic interventions
  • Research Contribution: Advances understanding of rare neurological disorders

Understanding Your Test Results

Our comprehensive genetic counseling services help you interpret your ST3GAL3 test results:

  • Positive Result: Indicates the presence of pathogenic ST3GAL3 variants, confirming diagnosis
  • Negative Result: Suggests ST3GAL3 mutations are not the cause of symptoms
  • Variant of Uncertain Significance: Requires further clinical correlation and family studies
  • Carrier Status: Important information for family members and reproductive planning

Test Pricing and Details

Test Feature Details
Test Name ST3GAL3 Gene Early Infantile Epileptic Encephalopathy Type 15 NGS Genetic DNA Test
Regular Price $700 USD
Discount Price $500 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 ST3GAL3 genetic test, we recommend:

  • Complete clinical history documentation of the patient
  • Genetic counseling session to create detailed family pedigree
  • Neurological evaluation and EEG results
  • Discussion of test implications with healthcare providers

Nationwide Testing Availability

We provide comprehensive genetic testing services across the United States with convenient locations in major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art laboratories ensure consistent, high-quality results regardless of your location.

Take the Next Step Toward Answers

If your child is experiencing symptoms of early infantile epileptic encephalopathy, don’t wait to get the answers you need. Our specialized ST3GAL3 genetic test provides the clarity required for proper diagnosis and treatment planning. Contact our genetic counselors today to discuss your specific situation and schedule testing.

Call or WhatsApp: +1(267) 388-9828 to book your ST3GAL3 Gene Early Infantile Epileptic Encephalopathy Type 15 NGS Genetic DNA Test today. Our compassionate team is ready to guide you through the testing process and help you understand your results.