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OTOA Gene Deafness Autosomal Recessive Type 22 Genetic Test

Original price was: $700.Current price is: $500.

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The OTOA Gene Deafness Autosomal Recessive Type 22 NGS Genetic DNA Test is a comprehensive diagnostic examination that identifies mutations in the OTOA gene responsible for hereditary hearing impairment. This advanced genetic test utilizes next-generation sequencing technology to detect specific genetic variations associated with autosomal recessive deafness type 22. The test is particularly valuable for individuals with family history of hearing loss, children with unexplained hearing impairment, and couples planning pregnancy with known genetic risk factors. Results provide crucial information for early intervention strategies, hearing management approaches, and informed family planning decisions. The test is available for $500 USD with a regular price of $700 USD, offering significant savings for comprehensive genetic analysis.

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OTOA Gene Deafness Autosomal Recessive Type 22 NGS Genetic DNA Test

Understanding OTOA Gene-Related Hearing Loss

The OTOA Gene Deafness Autosomal Recessive Type 22 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for hereditary hearing disorders. This comprehensive examination focuses on identifying mutations within the OTOA gene, which plays a critical role in the development and function of the inner ear structures essential for normal hearing. Autosomal recessive type 22 deafness is a specific genetic condition characterized by progressive or congenital hearing impairment that follows an autosomal recessive inheritance pattern, meaning both copies of the gene must contain mutations for the condition to manifest.

What Does This Genetic Test Measure?

This advanced diagnostic test specifically targets and analyzes the OTOA gene using next-generation sequencing (NGS) technology to detect:

  • Point mutations and single nucleotide variants within the OTOA gene
  • Small insertions and deletions that may disrupt gene function
  • Copy number variations affecting the OTOA gene region
  • Pathogenic variants associated with autosomal recessive hearing loss type 22
  • Genetic markers predictive of hearing impairment progression

Who Should Consider OTOA Gene Testing?

Clinical Indications and Symptoms

This genetic test is particularly recommended for individuals experiencing:

  • Unexplained congenital or early-onset hearing loss
  • Progressive hearing deterioration without clear environmental causes
  • Family history of hereditary hearing impairment
  • Children with delayed speech development due to hearing issues
  • Individuals with consanguineous parents or family background
  • Couples planning pregnancy with known family history of genetic hearing disorders
  • Patients with sensorineural hearing loss of unknown etiology

Comprehensive Benefits of Genetic Testing

Undergoing the OTOA Gene Deafness Test provides numerous advantages for patients and families:

  • Early Intervention Opportunities: Enables proactive hearing management strategies before significant impairment occurs
  • Accurate Diagnosis: Provides definitive genetic confirmation of hearing loss etiology
  • Family Planning Guidance: Informs reproductive decisions and genetic counseling
  • Personalized Treatment Approaches: Guides appropriate hearing aid selection and rehabilitation strategies
  • Psychological Relief: Reduces uncertainty and provides clarity about hearing condition
  • Research Contribution: Advances understanding of genetic hearing disorders

Understanding Your Test Results

Interpretation Guidance

Your genetic test results will fall into one of several categories with specific implications:

  • Positive Result: Identification of pathogenic mutations in both OTOA gene copies confirms diagnosis of autosomal recessive deafness type 22
  • Carrier Status: Detection of a single mutated copy indicates carrier status without clinical symptoms
  • Negative Result: No pathogenic variants detected suggests OTOA gene is not the cause of hearing issues
  • Variant of Uncertain Significance: Genetic changes with unknown clinical impact requiring further evaluation

All results include comprehensive genetic counseling to ensure proper understanding and appropriate next steps. Our certified genetic counselors provide detailed explanations and support for result interpretation.

Test Pricing and Availability

Test Component Price (USD)
Discount Price $500
Regular Price $700
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card

Pre-Test Requirements

Before testing, patients should provide:

  • Complete clinical history including hearing assessment records
  • Family medical history with emphasis on hearing disorders
  • Participation in genetic counseling session to create detailed pedigree chart
  • Informed consent for genetic testing and result disclosure

Nationwide Testing Availability

General Genetics Corporation provides comprehensive OTOA gene testing services across the United States with convenient locations in all major metropolitan areas. Our state-of-the-art genetic testing facilities ensure accurate results and professional service delivery. We maintain partnerships with leading ENT specialists and genetic medicine departments to provide integrated care for patients with hereditary hearing conditions.

Take Control of Your Hearing Health Today

Don’t let uncertainty about hereditary hearing conditions affect your quality of life. The OTOA Gene Deafness Autosomal Recessive Type 22 NGS Genetic DNA Test provides definitive answers and empowers informed healthcare decisions. Our experienced genetic specialists and ENT consultants are ready to guide you through the testing process and help interpret your results.

Schedule your genetic consultation and testing appointment today by calling our dedicated genetics hotline at +1(267) 388-9828 or book online through our secure patient portal. Take the first step toward understanding your genetic hearing health with confidence and clarity.