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 groundbreaking diagnostic tool designed to identify genetic mutations responsible for hearing loss. This test employs Next Generation Sequencing (NGS) technology, which allows for a comprehensive analysis of the WHRN gene, crucial for normal auditory function. With the increasing prevalence of genetic hearing disorders, this test plays a vital role in early diagnosis and management.
What the Test Measures
This genetic test specifically measures mutations in the WHRN gene, which is associated with autosomal recessive deafness. By detecting these mutations, healthcare providers can determine the underlying cause of hearing impairment, allowing for tailored treatment plans.
Who Should Consider This Test?
This test is recommended for individuals who:
- Have a family history of hearing loss.
- Experience unexplained hearing impairment.
- Are planning a family and want to understand potential genetic risks.
- Have been advised by an ENT doctor or genetic counselor.
Benefits of Taking the Test
- Accurate diagnosis of genetic hearing loss.
- Informed family planning decisions.
- Guidance for appropriate interventions and treatments.
- Increased understanding of potential hereditary risks.
Understanding Your Results
Results from the WHRN Gene Deafness Test are typically available within 3 to 4 weeks. A genetic counselor will assist in interpreting the results, providing insights into the implications for the patient and their family. It is essential to discuss the results with your healthcare provider to understand the next steps.
Test Pricing
| Price Type | Amount (KSh) |
|---|---|
| Discount Price | 40,000 |
| Regular Price | 56,000 |
Branches and Booking
We have branches across all major cities in Kenya, including Nairobi, Mombasa, Kisumu, and more. Our team is ready to assist you with the WHRN Gene Deafness Autosomal Recessive Type 31 NGS Genetic DNA Test. To book the test, please call or WhatsApp us at +254711564616.
Sample Type and Pre-Test Instructions
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card.
Pre-test instructions include a clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test.
Conclusion
The WHRN Gene Deafness Autosomal Recessive Type 31 NGS Genetic DNA Test is a critical step in understanding and managing genetic hearing loss. By taking this test, you can gain valuable insights into your health and the health of your family.
