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DIAPH1 Gene Deafness Autosomal Dominant Type 1 Genetic Test

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

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The DIAPH1 Gene Deafness Autosomal Dominant Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the DIAPH1 gene responsible for hereditary hearing loss. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect specific genetic variations that cause autosomal dominant nonsyndromic hearing loss. The test is particularly valuable for individuals with family history of hearing impairment, those experiencing progressive hearing loss, and couples planning pregnancy with genetic risk factors. Results provide crucial information for early intervention, treatment planning, and genetic counseling. The test is available for $500 USD (discounted from $700 USD) with results delivered within 3-4 weeks.

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DIAPH1 Gene Deafness Autosomal Dominant Type 1 NGS Genetic DNA Test

Understanding DIAPH1 Gene-Related Hearing Loss

The DIAPH1 Gene Deafness Autosomal Dominant Type 1 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for hereditary hearing disorders. This advanced test specifically targets mutations in the DIAPH1 gene, which plays a crucial role in the development and function of the inner ear. Autosomal dominant nonsyndromic hearing loss type 1 (DFNA1) is characterized by progressive sensorineural hearing impairment that typically begins in childhood and worsens over time.

What Does This Test Measure?

Our comprehensive NGS-based genetic test analyzes the entire coding region of the DIAPH1 gene to identify pathogenic variants responsible for autosomal dominant hearing loss. The test detects:

  • Point mutations and single nucleotide variants
  • Small insertions and deletions
  • Copy number variations
  • Splice site mutations
  • Regulatory region abnormalities

Who Should Consider This Genetic Test?

This test is recommended for individuals experiencing specific symptoms or with particular risk factors:

Clinical Indications

  • Progressive hearing loss beginning in childhood or early adulthood
  • Family history of hereditary hearing impairment
  • Unexplained sensorineural hearing loss
  • Individuals planning pregnancy with family history of hearing disorders
  • Children with delayed speech development due to hearing issues
  • Patients with bilateral symmetrical hearing loss

Key Symptoms That Warrant Testing

  • Gradual worsening of hearing ability over time
  • Difficulty understanding speech in noisy environments
  • High-frequency hearing loss
  • Tinnitus accompanying hearing impairment
  • Family members diagnosed with genetic hearing conditions

Benefits of DIAPH1 Genetic Testing

Early Detection and Intervention

Identifying DIAPH1 gene mutations enables early intervention strategies that can significantly improve quality of life. Early detection allows for:

  • Timely hearing aid fitting and cochlear implant consideration
  • Appropriate educational and communication support
  • Preventive measures to protect remaining hearing
  • Family planning decisions and genetic counseling

Personalized Treatment Planning

Genetic confirmation provides valuable information for developing targeted treatment approaches:

  • Customized hearing rehabilitation programs
  • Monitoring protocols for progressive hearing loss
  • Genetic counseling for family members
  • Informed decisions about medical management

Understanding Your Test Results

Positive Result Interpretation

A positive result indicates the presence of a pathogenic mutation in the DIAPH1 gene. This confirms the genetic basis of hearing loss and enables:

  • Accurate diagnosis and prognosis
  • Family member testing recommendations
  • Personalized management strategies
  • Reproductive planning guidance

Negative Result Interpretation

A negative result suggests that no pathogenic DIAPH1 mutations were detected. However, this doesn’t completely rule out genetic hearing loss, as other genes may be involved. Further testing may be recommended based on clinical presentation.

Variant of Uncertain Significance (VUS)

Some genetic changes may be classified as VUS, meaning their clinical significance is currently unknown. In such cases, periodic re-evaluation and family studies may be recommended.

Test Details and Pricing

Test Information Details
Test Name DIAPH1 Gene Deafness Autosomal Dominant Type 1 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

Pre-Test Requirements

Before undergoing testing, we recommend:

  • Comprehensive clinical history documentation
  • Genetic counseling session to discuss implications
  • Family pedigree analysis for hereditary patterns
  • Understanding of potential outcomes and limitations

Nationwide Testing Availability

We have conveniently located branches 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 state-of-the-art genetic testing facilities ensure accurate and reliable results nationwide.

Take Control of Your Hearing Health

Don’t let uncertainty about hereditary hearing loss affect your quality of life. Our DIAPH1 genetic test provides definitive answers and empowers you to make informed decisions about your hearing health and family planning.

Ready to Schedule Your Test?

Contact our genetic specialists today to schedule your DIAPH1 Gene Deafness Autosomal Dominant Type 1 NGS Genetic DNA Test. Our team is available to answer your questions and guide you through the testing process.

Call or WhatsApp: +1(267) 388-9828

Book your appointment now and take the first step toward understanding your genetic hearing health. Early detection through genetic testing can make a significant difference in managing hereditary hearing conditions effectively.