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NR2E1 Gene Polymicrogyria Bilateral Occipital NGS Genetic DNA Test

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

-29%

The NR2E1 Gene Polymicrogyria Bilateral Occipital NGS Genetic DNA Test is a cutting-edge genetic diagnostic tool that identifies mutations in the NR2E1 gene associated with bilateral occipital polymicrogyria. This specialized test utilizes Next-Generation Sequencing (NGS) technology to detect genetic abnormalities that cause brain malformations, particularly affecting the occipital lobes. The test is crucial for children showing developmental delays, seizures, or visual processing difficulties. Priced at $500 USD (discounted from $700), this comprehensive analysis provides definitive diagnosis, enables personalized treatment planning, and offers valuable information for family genetic counseling. Results are typically available within 3-4 weeks from sample collection.

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NR2E1 Gene Polymicrogyria Bilateral Occipital NGS Genetic DNA Test

Comprehensive Genetic Testing for Brain Malformation Disorders

The NR2E1 Gene Polymicrogyria Bilateral Occipital NGS Genetic DNA Test represents a breakthrough in pediatric neurology and genetic diagnostics. This advanced testing method specifically targets the NR2E1 gene, which plays a critical role in brain development and cortical organization. Polymicrogyria is a complex brain malformation characterized by excessive folding of the cerebral cortex with abnormal small gyri, particularly affecting the occipital lobes responsible for visual processing.

What This Test Measures and Detects

Our specialized NGS genetic test precisely identifies:

  • Mutations in the NR2E1 gene associated with bilateral occipital polymicrogyria
  • Specific genetic variants affecting brain cortical development
  • Inheritance patterns of polymicrogyria-related genetic conditions
  • Risk assessment for family members through comprehensive genetic analysis

Who Should Consider This Test

This genetic test is recommended for individuals presenting with:

  • Developmental delays in infancy or early childhood
  • Seizures or epilepsy of unknown origin
  • Visual processing difficulties or cortical visual impairment
  • Abnormal brain MRI findings showing polymicrogyria
  • Family history of brain malformations or neurological disorders
  • Unexplained intellectual disability in children
  • Motor coordination challenges and movement disorders

Key Benefits of NR2E1 Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Definitive Diagnosis: Confirms or rules out NR2E1-related polymicrogyria
  • Personalized Treatment Planning: Enables targeted therapeutic interventions
  • Family Genetic Counseling: Provides crucial information for reproductive planning
  • Early Intervention: Facilitates timely developmental support services
  • Prognostic Information: Helps understand potential developmental outcomes
  • Research Contribution: Advances understanding of rare neurological conditions

Understanding Your Test Results

Our genetic counseling team provides comprehensive result interpretation:

  • Positive Result: Indicates presence of NR2E1 gene mutation associated with polymicrogyria
  • Negative Result: Suggests absence of tested NR2E1 mutations
  • Variant of Uncertain Significance: Requires additional family studies and clinical correlation
  • Carrier Status: Important for family planning and genetic counseling

All results are accompanied by detailed explanations from our certified genetic counselors, ensuring you fully understand the implications for your child’s health and development.

Test Pricing and Details

Test Component Details
Test Name NR2E1 Gene Polymicrogyria Bilateral Occipital 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

To ensure accurate testing and comprehensive care:

  • Complete clinical history of the patient
  • Genetic counseling session to create detailed family pedigree
  • Documentation of affected family members with similar conditions
  • Previous neurological evaluations and brain imaging reports

Nationwide Accessibility

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, San Jose, and many more. Our network of certified genetic counselors and pediatric neurologists ensures you receive expert care regardless of your location.

Take the Next Step Toward Answers

If your child is experiencing symptoms suggestive of polymicrogyria or has unexplained neurological challenges, don’t wait to get answers. Our NR2E1 genetic test provides the clarity needed for proper diagnosis and treatment planning.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book the NR2E1 Gene Polymicrogyria Bilateral Occipital NGS Genetic DNA Test. Our compassionate team is ready to guide you through every step of the testing process and help you understand what the results mean for your child’s future.

Early genetic diagnosis can make a significant difference in managing neurological conditions and optimizing developmental outcomes. Trust the experts at General Genetics Corporation for accurate, reliable genetic testing you can depend on.