NR2E1 Gene Polymicrogyria Bilateral Occipital NGS Genetic DNA Test
Comprehensive Genetic Testing for Neurological Development Disorders
The NR2E1 Gene Polymicrogyria Bilateral Occipital NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise identification of mutations associated with bilateral occipital polymicrogyria. This sophisticated testing methodology provides crucial insights for patients and families affected by complex neurological development conditions.
What This Advanced Genetic Test Measures
Our comprehensive NGS genetic analysis specifically targets the NR2E1 gene, which plays a critical role in brain development and cortical organization. The test detects:
- Point mutations and small insertions/deletions in the NR2E1 gene
- Genetic variations associated with bilateral occipital polymicrogyria
- Inheritance patterns that may affect family planning decisions
- Specific genetic markers linked to neurological development disorders
Who Should Consider This Genetic Test
This specialized genetic testing is recommended for individuals presenting with:
- Developmental delays in motor skills or cognitive function
- Visual processing difficulties or cortical visual impairment
- Seizures or epilepsy with unknown etiology
- Family history of neurological disorders or polymicrogyria
- Abnormal brain imaging showing cortical malformations
- Unexplained intellectual disability or learning challenges
Significant Benefits of Genetic Testing
Undergoing the NR2E1 genetic test provides numerous advantages for patients and healthcare providers:
- Accurate Diagnosis: Provides definitive identification of genetic causes for neurological symptoms
- Personalized Treatment: Enables targeted therapeutic approaches based on genetic findings
- Family Planning Guidance: Offers crucial information for genetic counseling and reproductive decisions
- Prognostic Insights: Helps predict disease progression and potential complications
- Early Intervention: Facilitates timely implementation of supportive therapies and educational strategies
Understanding Your Test Results
Our comprehensive genetic counseling services help you interpret your results effectively:
- Positive Result: Indicates the presence of NR2E1 gene mutations associated with polymicrogyria, requiring specialized neurological care and management
- Negative Result: Suggests that NR2E1 mutations are not the cause of symptoms, guiding further diagnostic investigations
- Variant of Uncertain Significance: Identifies genetic changes requiring additional research and follow-up testing
- Carrier Status: Provides information about inheritance patterns and family risk assessment
Test Pricing and Availability
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Accessibility
We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, and many other cities. Our network of certified genetic counselors and neurological specialists ensures comprehensive care regardless of your location.
Take the Next Step Toward Genetic Clarity
Don’t let uncertainty about neurological symptoms affect your quality of life. Our NR2E1 Gene Polymicrogyria Bilateral Occipital NGS Genetic DNA Test provides the answers you need for informed medical decisions and personalized care planning.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic testing appointment and take control of your neurological health journey.
Our dedicated team of genetic specialists is ready to guide you through the testing process, from initial consultation to comprehensive result interpretation and ongoing support.
