WHRN Gene Deafness Autosomal Recessive Type 31 NGS Genetic DNA Test
Introduction
The WHRN Gene Deafness Autosomal Recessive Type 31 NGS Genetic DNA Test is a specialized diagnostic tool designed to identify genetic mutations associated with hearing loss. This test leverages Next-Generation Sequencing (NGS) technology to provide accurate and comprehensive results, essential for individuals experiencing unexplained deafness. Understanding the genetic basis of hearing impairment can significantly impact treatment options and family planning.
What the Test Measures
This genetic test specifically detects mutations in the WHRN gene, which is known to play a critical role in the development of auditory function. By analyzing the DNA, the test can confirm or rule out the presence of genetic factors contributing to autosomal recessive deafness.
Who Should Consider This Test
Individuals who should consider the WHRN Gene Deafness Test include:
- Those with a family history of hearing loss.
- Individuals experiencing unexplained deafness or hearing impairment.
- Patients with clinical indications of genetic hearing loss as advised by an ENT doctor.
Benefits of Taking the Test
Taking the WHRN Gene Deafness Test offers numerous benefits, including:
- Accurate diagnosis of genetic hearing loss.
- Informed family planning decisions for affected families.
- Guidance on potential treatment options and interventions.
- Access to genetic counseling for better understanding of results.
Understanding Your Results
Results from the WHRN Gene Deafness Test will provide insights into the presence of genetic mutations. A genetic counselor will assist in interpreting these results, discussing their implications for the patient and their family. It is essential to understand that not all genetic mutations lead to hearing loss, and further evaluation may be necessary.
Test Price
Price Type | Amount (NGN) |
---|---|
Discount Price | 400,000 NGN |
Regular Price | 560,000 NGN |
Booking the Test
To book the WHRN Gene Deafness Autosomal Recessive Type 31 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you in scheduling your appointment and providing any additional information you may need.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Clinical history of the patient who is going for the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A genetic counseling session to draw a pedigree chart of family members affected with the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN30.