STRC Gene Deafness Autosomal Recessive Type 16 NGS Genetic DNA Test
Comprehensive Genetic Analysis for Hereditary Hearing Loss
The STRC Gene Deafness Autosomal Recessive Type 16 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for hearing disorders. This advanced test utilizes Next-Generation Sequencing (NGS) technology to identify mutations in the STRC (stereocilin) gene, which plays a crucial role in the structure and function of hair cells in the inner ear. Understanding your genetic predisposition to hearing loss can provide invaluable insights for medical management, family planning, and early intervention strategies.
What Does This Test Measure and Detect?
This comprehensive genetic analysis specifically targets:
- Mutations in the STRC gene located on chromosome 15q15.3
- Autosomal recessive inheritance patterns for deafness type 16 (DFNB16)
- Pathogenic variants affecting stereocilin protein function
- Copy number variations and deletions in the STRC gene region
- Genetic markers associated with prelingual non-syndromic hearing loss
Who Should Consider This Genetic Test?
This test is particularly recommended for individuals experiencing:
- Unexplained childhood or congenital hearing loss
- Family history of hereditary deafness without known cause
- Progressive hearing impairment starting in early childhood
- Planning for pregnancy with family history of hearing disorders
- Diagnostic uncertainty regarding the etiology of hearing loss
- Siblings of individuals with confirmed STRC gene mutations
Clinical Symptoms and Indications
Patients may present with various symptoms including:
- Bilateral sensorineural hearing loss typically manifesting in infancy
- Moderate to severe hearing impairment affecting speech development
- Non-syndromic hearing loss without associated systemic features
- Progressive deterioration of hearing function in some cases
- Normal vestibular function despite significant hearing impairment
Benefits of STRC Gene Testing
Early Intervention and Management
Genetic testing for STRC mutations provides numerous advantages:
- Accurate Diagnosis: Precise identification of the genetic cause of hearing loss
- Family Planning Guidance: Understanding inheritance risks for future generations
- Personalized Treatment: Tailored hearing rehabilitation and management strategies
- Early Intervention: Opportunity for timely hearing aid fitting or cochlear implantation
- Genetic Counseling: Comprehensive support for understanding test results and implications
- Peace of Mind: Resolution of diagnostic uncertainty and appropriate medical guidance
Understanding Your Test Results
Interpretation Guidelines
Your genetic test results will be carefully interpreted by our expert genetic counselors:
Positive Result
- Confirmation of pathogenic STRC gene mutations
- Diagnosis of autosomal recessive deafness type 16
- Recommendations for hearing management and family screening
- Referral to appropriate specialists for comprehensive care
Negative Result
- No detected mutations in the STRC gene
- Consideration of alternative genetic causes of hearing loss
- Continued monitoring if clinical symptoms persist
- Discussion of additional testing options if indicated
Variant of Uncertain Significance (VUS)
- Identification of genetic changes with unknown clinical impact
- Recommendations for family studies to clarify significance
- Periodic re-evaluation as scientific knowledge advances
- Clinical correlation with patient symptoms and family history
Test Details and Pricing
| Test Parameter | Details |
|---|---|
| Test Name | STRC Gene Deafness Autosomal Recessive Type 16 NGS Genetic DNA Test |
| Regular Price | $700 USD |
| Discount Price | $500 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 | ENT Doctor, Genetics Department |
| Disease Category | Ear Nose Throat Disorders |
Pre-Test Preparation and Requirements
Essential Pre-Test Instructions
To ensure optimal testing conditions and accurate results:
- Complete clinical history documentation including hearing loss patterns
- Genetic counseling session to create detailed family pedigree chart
- Documentation of affected family members with hearing disorders
- Review of previous audiological evaluations and test results
- Discussion of testing implications and potential outcomes
- Informed consent process for genetic testing
Nationwide Testing Availability
We are proud to offer comprehensive genetic testing services across the United States with convenient locations in all major metropolitan areas including:
- New York City and surrounding tri-state area
- Los Angeles and Southern California region
- Chicago and Midwest locations
- Houston, Dallas, and Texas facilities
- Miami, Orlando, and Florida centers
- Seattle, Portland, and Pacific Northwest clinics
- Boston, Philadelphia, and Northeast locations
- Atlanta, Charlotte, and Southeast testing centers
Take Control of Your Hearing Health Today
Don’t let uncertainty about hereditary hearing loss affect your quality of life. Our STRC Gene Deafness Autosomal Recessive Type 16 NGS Genetic DNA Test provides the clarity and answers you need for informed healthcare decisions. With our discounted price of $500 USD and comprehensive genetic counseling support, you can access cutting-edge genetic diagnostics with confidence.
Ready to schedule your test? Contact our genetic specialists today at +1(267) 388-9828 or visit one of our conveniently located testing centers nationwide. Our team is available to answer your questions, schedule appointments, and provide the support you need throughout the testing process.
Early detection through genetic testing can make a significant difference in managing hearing health and planning for the future. Take the first step toward understanding your genetic profile and protecting your hearing wellness.
