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POU3F4 Gene Deafness X-Linked Type 2 Genetic Test

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

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The POU3F4 Gene Deafness X-Linked Type 2 NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the POU3F4 gene responsible for X-linked nonsyndromic hearing loss. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to provide accurate detection of genetic variants associated with progressive sensorineural hearing impairment. The test is particularly valuable for individuals with family history of hearing loss, children with unexplained deafness, or adults experiencing progressive hearing deterioration. Results help guide treatment decisions, inform family planning, and provide crucial genetic counseling information. The test is available for $500 USD and provides results within 3-4 weeks using blood, extracted DNA, or blood spot samples.

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POU3F4 Gene Deafness X-Linked Type 2 NGS Genetic DNA Test

Comprehensive Genetic Analysis for Hereditary Hearing Loss

The POU3F4 Gene Deafness X-Linked Type 2 NGS Genetic DNA Test represents a breakthrough in molecular diagnostics for hereditary hearing disorders. This advanced genetic screening utilizes state-of-the-art Next-Generation Sequencing technology to identify specific mutations in the POU3F4 gene, which plays a critical role in auditory system development and function. Understanding your genetic predisposition to hearing loss can provide invaluable insights for proactive healthcare management and informed family planning decisions.

What This Test Measures and Detects

This comprehensive genetic analysis specifically targets the POU3F4 gene located on the X chromosome, which encodes a transcription factor essential for proper inner ear development. The test identifies:

  • Pathogenic variants in the POU3F4 gene associated with DFNX2 nonsyndromic hearing loss
  • Point mutations, deletions, and insertions affecting gene function
  • X-linked inheritance patterns of hearing impairment
  • Genetic markers for progressive sensorineural hearing loss
  • Risk assessment for congenital or childhood-onset deafness

Who Should Consider This Genetic Test

This test is particularly recommended for individuals experiencing:

  • Unexplained progressive hearing loss beginning in childhood
  • Family history of X-linked hearing impairment patterns
  • Males with congenital or early-onset sensorineural hearing loss
  • Individuals with mixed hearing loss involving both conductive and sensorineural components
  • Patients with abnormal temporal bone imaging findings
  • Couples planning pregnancy with family history of hereditary deafness
  • Children with delayed speech development due to hearing issues

Key Benefits of POU3F4 Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Accurate Diagnosis: Confirms genetic basis of hearing loss, eliminating diagnostic uncertainty
  • Family Planning Guidance: Provides crucial information for genetic counseling and reproductive decisions
  • Personalized Management: Enables targeted interventions and appropriate hearing rehabilitation strategies
  • Early Intervention: Facilitates timely implementation of hearing aids, cochlear implants, or communication therapies
  • Risk Assessment: Identifies at-risk family members for proactive monitoring
  • Research Contribution: Advances understanding of genetic hearing disorders

Understanding Your Test Results

Your genetic test results will be carefully interpreted by our expert genetic counselors and ENT specialists:

  • Positive Result: Indicates presence of pathogenic POU3F4 mutation, confirming X-linked deafness diagnosis
  • Negative Result: Suggests absence of tested mutations, though other genetic or environmental factors may contribute to hearing loss
  • Variant of Uncertain Significance: Requires additional family studies and clinical correlation
  • Carrier Status: Important information for female relatives regarding transmission risk

All results include comprehensive genetic counseling to ensure proper understanding and appropriate next steps.

Test Pricing and Details

Test Component Details
Test Name POU3F4 Gene Deafness X-Linked Type 2 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

Nationwide Accessibility

We have branches conveniently located across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our state-of-the-art genetic testing facilities ensure consistent, high-quality results regardless of your location.

Take Control of Your Hearing Health Today

Don’t let uncertainty about hereditary hearing loss impact your quality of life. Our comprehensive POU3F4 genetic testing provides the clarity you need to make informed healthcare decisions. With our discounted price of $500 and rapid 3-4 week turnaround, there’s never been a better time to understand your genetic profile.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our expert team is ready to guide you through every step of the process and help you achieve better hearing health outcomes.