FGF3 Gene Deafness Congenital with Inner Ear Agenesis Microtia and Microdontia NGS Genetic DNA Test
Comprehensive Genetic Analysis for Congenital Hearing Disorders
The FGF3 Gene Deafness Congenital with Inner Ear Agenesis Microtia and Microdontia NGS Genetic DNA Test represents a breakthrough in molecular diagnostics for individuals affected by complex congenital hearing disorders. This specialized genetic test utilizes cutting-edge Next-Generation Sequencing (NGS) technology to identify mutations in the FGF3 (Fibroblast Growth Factor 3) gene, which plays a critical role in embryonic development of the inner ear structures.
What This Test Measures and Detects
This comprehensive genetic analysis specifically targets:
- Mutations in the FGF3 gene associated with congenital deafness
- Genetic variations causing inner ear agenesis (complete absence of inner ear structures)
- Molecular markers for microtia (underdeveloped or absent external ears)
- Genetic factors contributing to microdontia (abnormally small teeth)
- Inheritance patterns and carrier status for family planning
Who Should Consider This Test
This genetic screening is recommended for individuals presenting with:
- Congenital hearing loss or deafness from birth
- Abnormal inner ear development detected through imaging studies
- Microtia (malformed or absent external ears)
- Microdontia or dental abnormalities alongside hearing issues
- Family history of congenital hearing disorders
- Unexplained sensorineural hearing loss in childhood
- Multiple congenital anomalies involving ear development
Clinical Benefits of FGF3 Genetic Testing
Undergoing this specialized genetic analysis provides numerous advantages:
- Accurate Diagnosis: Precise identification of the underlying genetic cause of hearing disorders
- Personalized Treatment Planning: Tailored intervention strategies based on specific genetic findings
- Family Planning Guidance: Understanding inheritance patterns for future family decisions
- Early Intervention: Opportunity for timely management and support services
- Comprehensive Care Coordination: Integration with ENT specialists and genetic counselors
Understanding Your Test Results
Your genetic test results will be thoroughly explained by our certified genetic counselors:
- Positive Result: Indicates the presence of FGF3 gene mutations associated with the disorder
- Negative Result: Suggests no detectable mutations in the FGF3 gene analyzed
- Variant of Uncertain Significance: Identifies genetic changes with unclear clinical implications
- Carrier Status: Determines if you carry one copy of a mutated gene
All results include detailed interpretation and recommendations for next steps in management and follow-up care.
Test Pricing and Availability
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
We have diagnostic centers conveniently located across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified genetic testing facilities ensures accessible, high-quality care for patients nationwide.
Book Your Genetic Consultation Today
Take the first step toward understanding your genetic health. Our team of expert genetic counselors and ENT specialists are ready to provide comprehensive care and support throughout your testing journey.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your FGF3 genetic testing appointment. Our dedicated patient coordinators will assist you with insurance verification, appointment scheduling, and answer any questions about the testing process.
Turnaround Time: 3 to 4 Weeks | Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card
