HOXB1 Gene Facial Paresis Type 3 NGS Genetic DNA Test
Comprehensive Genetic Testing for Hereditary Facial Paralysis
The HOXB1 Gene Facial Paresis Type 3 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise identification of mutations responsible for hereditary facial paralysis conditions. This advanced testing utilizes next-generation sequencing (NGS) technology to provide comprehensive analysis of the HOXB1 gene, which plays a critical role in facial nerve development and function.
What Does This Test Measure?
This specialized genetic test specifically targets and analyzes the HOXB1 gene for mutations associated with Facial Paresis Type 3, a rare hereditary neurological disorder. The test examines:
- Complete sequencing of the HOXB1 gene coding regions
- Detection of point mutations, insertions, and deletions
- Identification of pathogenic variants linked to facial nerve dysfunction
- Assessment of genetic markers for hereditary transmission patterns
Who Should Consider This Test?
This genetic screening is particularly recommended for individuals experiencing:
- Unexplained facial weakness or paralysis
- Family history of facial paresis or similar neurological conditions
- Congenital facial asymmetry or movement limitations
- Progressive facial muscle weakness without clear cause
- Multiple family members affected by facial nerve disorders
- Children with developmental facial movement abnormalities
Key Benefits of HOXB1 Genetic Testing
- Definitive Diagnosis: Provides conclusive evidence of genetic predisposition to facial paresis
- Family Planning Guidance: Enables informed reproductive decisions for affected families
- Personalized Treatment: Helps neurologists develop targeted management strategies
- Early Intervention: Allows for proactive symptom management and therapy planning
- Genetic Counseling: Supports comprehensive family risk assessment and education
Understanding Your Test Results
Your HOXB1 genetic test results will fall into one of several categories:
- Positive Result: Indicates the presence of a known pathogenic mutation in the HOXB1 gene, confirming genetic predisposition to Facial Paresis Type 3
- Negative Result: Suggests no detectable mutations in the HOXB1 gene, though other genetic or non-genetic causes should still be considered
- Variant of Uncertain Significance: Identifies genetic changes with unknown clinical implications, requiring further evaluation and family studies
- Carrier Status: May identify individuals who carry the mutation but may not show symptoms
Test Details and Pricing
| Test Feature | Details |
|---|---|
| Test Name | HOXB1 Gene Facial Paresis Type 3 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 |
| Specialty | Neurology & Genetics |
Pre-Test Requirements
Before undergoing the HOXB1 genetic test, patients should provide:
- Complete clinical history detailing facial paralysis symptoms and progression
- Participation in a genetic counseling session to create a detailed family pedigree chart
- Documentation of affected family members and their relationship to the patient
- Previous neurological evaluations and test results, if available
Nationwide Testing Availability
We have comprehensive testing facilities across the United States, with branches in all 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 Control of Your Neurological Health
Don’t let uncertainty about hereditary facial paralysis affect your quality of life. The HOXB1 Gene Facial Paresis Type 3 NGS Genetic DNA Test provides the clarity needed for effective management and informed family planning decisions. Our team of neurological genetic specialists is ready to support you through every step of the testing process.
Ready to schedule your test? Call or WhatsApp us today at +1(267) 388-9828 to book your appointment and take the first step toward understanding your genetic health.
