RAB3GAP2 Gene Warburg Micro Syndrome Type 2 NGS Genetic DNA Test
Comprehensive Genetic Testing for Rare Neurological Disorders
The RAB3GAP2 Gene Warburg Micro Syndrome Type 2 NGS Genetic DNA Test represents a breakthrough in molecular diagnostics for rare genetic conditions affecting neurological development. This specialized test utilizes advanced Next-Generation Sequencing (NGS) technology to analyze the RAB3GAP2 gene, which plays a crucial role in vesicle trafficking and neurotransmitter release within the central nervous system.
What Does This Test Measure?
Our comprehensive genetic analysis specifically targets the RAB3GAP2 gene to identify pathogenic variants associated with Warburg Micro Syndrome Type 2. The test examines:
- Complete coding regions of the RAB3GAP2 gene
- Exon-intron boundaries for splice site mutations
- Copy number variations and structural rearrangements
- Point mutations, insertions, and deletions
- Autosomal recessive inheritance patterns
Who Should Consider This Test?
This genetic test is recommended for individuals presenting with the following clinical features:
- Congenital cataracts or other ocular abnormalities
- Microcephaly (abnormally small head circumference)
- Global developmental delays and intellectual disability
- Hypotonia progressing to spasticity
- Seizures or epilepsy
- Corpus callosum abnormalities on brain imaging
- Family history of similar neurological conditions
- Consanguineous parentage with neurological symptoms
Clinical Benefits of Genetic Testing
Early and accurate diagnosis through RAB3GAP2 genetic testing provides numerous clinical advantages:
- Definitive Diagnosis: Confirms Warburg Micro Syndrome Type 2, eliminating diagnostic uncertainty
- Family Planning: Enables informed reproductive decisions and prenatal testing options
- Personalized Management: Guides appropriate medical interventions and therapeutic approaches
- Prognostic Information: Helps predict disease progression and potential complications
- Genetic Counseling: Provides comprehensive risk assessment for family members
- Research Contribution: Advances understanding of rare genetic disorders
Understanding Your Test Results
Our genetic testing provides detailed analysis with comprehensive interpretation:
- Positive Result: Identifies pathogenic variants in RAB3GAP2 gene confirming diagnosis
- Negative Result: No disease-causing mutations detected, though clinical correlation required
- Variant of Uncertain Significance: Identifies genetic changes with unclear clinical impact
- Carrier Status: Determines if individuals carry one copy of mutated gene
All results include detailed genetic counseling to ensure proper understanding and appropriate next steps for medical management.
Test Pricing and Availability
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
| Turnaround Time | 3-4 Weeks |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card |
Nationwide Testing Availability
We provide comprehensive genetic testing services across the United States with convenient 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 state-of-the-art laboratories ensure accurate and reliable results with full compliance to CLIA and CAP standards.
Pre-Test Requirements
Before scheduling your RAB3GAP2 genetic test, please ensure:
- Complete clinical history documentation
- Genetic counseling session scheduled
- Family pedigree chart prepared
- Informed consent obtained
- Insurance pre-authorization if applicable
Take Action Today
Don’t let diagnostic uncertainty delay proper medical care. Our specialized genetic testing provides the answers you need for effective management of Warburg Micro Syndrome Type 2. With our discounted price of $500 USD (regularly $700 USD), comprehensive genetic analysis is more accessible than ever.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your RAB3GAP2 genetic test and take the first step toward definitive diagnosis and personalized care.
Our experienced genetic counselors are available to discuss your specific situation, answer questions about the testing process, and help you understand how genetic testing can benefit you and your family. Early diagnosis leads to better outcomes – take control of your genetic health today.
