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TECTA Gene Deafness Autosomal Dominant Type 12 Genetic Test

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

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The TECTA Gene Deafness Autosomal Dominant Type 12 NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the TECTA gene responsible for autosomal dominant nonsyndromic hearing loss. This advanced next-generation sequencing test provides crucial information about hereditary hearing disorders, enabling early intervention and personalized management strategies. The test is particularly valuable for individuals with family history of hearing loss or those experiencing progressive hearing impairment. Results are typically available within 3-4 weeks, and the test requires either blood sample, extracted DNA, or one drop of blood on FTA card. At only $500 USD, this test offers affordable access to cutting-edge genetic diagnostics for hearing health.

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TECTA Gene Deafness Autosomal Dominant Type 12 NGS Genetic DNA Test

Understanding TECTA Gene-Related Hearing Loss

The TECTA Gene Deafness Autosomal Dominant Type 12 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for hereditary hearing disorders. This sophisticated test specifically targets mutations in the TECTA (tectorial membrane alpha) gene, which plays a critical role in the structure and function of the inner ear’s tectorial membrane. When this gene contains specific mutations, it can lead to autosomal dominant nonsyndromic hearing loss type 12 (DFNA12), a condition characterized by progressive hearing impairment that typically begins in childhood or early adulthood.

What This Advanced Genetic Test Detects

Our comprehensive NGS-based test meticulously analyzes the entire TECTA gene sequence to identify pathogenic variants responsible for autosomal dominant hearing loss. The test specifically detects:

  • Missense mutations affecting tectorial membrane protein structure
  • Nonsense mutations leading to premature protein termination
  • Frameshift mutations disrupting normal gene function
  • Splice site variants affecting mRNA processing
  • Copy number variations within the TECTA gene region

Who Should Consider TECTA Gene Testing?

This genetic test is particularly recommended for individuals experiencing:

  • Progressive hearing loss beginning in childhood or early adulthood
  • Family history of hereditary hearing impairment
  • High-frequency hearing loss that worsens over time
  • Unexplained sensorineural hearing loss without other symptoms
  • Individuals planning family with concerns about genetic transmission
  • Children with delayed speech development due to hearing issues

Clinical Indications and Symptoms

Patients typically present with bilateral sensorineural hearing loss that affects higher frequencies initially and progresses to involve mid and low frequencies. The hearing impairment often becomes noticeable during the first two decades of life and may show variable expressivity within families.

Significant Benefits of TECTA Gene Testing

Undergoing this genetic analysis provides numerous advantages for patients and families:

  • Accurate Diagnosis: Confirms genetic cause of hearing loss, eliminating diagnostic uncertainty
  • Family Planning Guidance: Provides crucial information for genetic counseling and reproductive decisions
  • Early Intervention: Enables timely implementation of hearing aids and communication strategies
  • Prognostic Information: Helps predict hearing loss progression and plan long-term management
  • Personalized Care: Facilitates tailored audiological management based on genetic findings
  • Psychological Relief: Reduces anxiety by providing definitive answers about hearing loss cause

Understanding Your Test Results

Our comprehensive genetic report provides clear, actionable information:

Positive Result Interpretation

A positive result indicates the presence of a pathogenic TECTA gene mutation. This confirms the genetic diagnosis of autosomal dominant nonsyndromic hearing loss type 12. Patients should:

  • Consult with an ENT specialist and genetic counselor
  • Implement appropriate hearing rehabilitation strategies
  • Inform family members about potential genetic risks
  • Schedule regular audiological evaluations

Negative Result Interpretation

A negative result suggests that no pathogenic TECTA mutations were detected. However, this doesn’t completely rule out genetic hearing loss, as other genes may be involved. Further evaluation may be recommended if clinical symptoms persist.

Variant of Uncertain Significance (VUS)

If a genetic change of unknown clinical significance is identified, ongoing research and family studies may help clarify its importance over time.

Test Pricing and Availability

Price Type Amount (USD)
Discount Price $500
Regular Price $700

Nationwide Accessibility

We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network of certified collection centers ensures easy access to this vital genetic testing service.

Take Control of Your Hearing Health Today

Don’t let uncertainty about hereditary hearing loss affect your quality of life. Our TECTA Gene Deafness Autosomal Dominant Type 12 NGS Genetic DNA Test provides the answers you need to make informed decisions about your hearing health and family planning. With results available in just 3-4 weeks and sample collection options including blood, extracted DNA, or simple blood spot cards, getting tested has never been more convenient.

Ready to take the next step? Call our genetic specialists today at +1(267) 388-9828 to schedule your appointment or book online through our secure patient portal. Early genetic testing can make a significant difference in managing hereditary hearing conditions effectively.