TRMU Gene Mitochondrial Modifier of Deafness NGS Genetic DNA Test
Introduction
The TRMU Gene Mitochondrial Modifier of Deafness NGS Genetic DNA Test is an advanced genetic diagnostic tool that plays a critical role in understanding the genetic factors contributing to hearing loss. This test utilizes Next Generation Sequencing (NGS) technology to analyze the TRMU gene, which has been implicated in mitochondrial functions that may affect auditory health.
What the Test Measures
This test specifically measures variations in the TRMU gene that may influence mitochondrial activity related to hearing. By identifying these genetic markers, healthcare providers can better understand the potential risk of deafness in individuals.
Who Should Consider This Test
This test is particularly recommended for individuals who:
- Have a family history of hearing loss or deafness.
- Exhibit symptoms such as difficulty hearing, tinnitus, or other auditory issues.
- Are undergoing evaluation for male infertility associated with CATSPER2 gene defects.
Benefits of Taking the Test
Taking the TRMU Gene Mitochondrial Modifier of Deafness NGS Genetic DNA Test offers several benefits:
- Provides clarity on genetic predispositions to deafness.
- Aids in family planning and genetic counseling by identifying at-risk family members.
- Guides treatment and management options for individuals with hearing disorders.
Understanding Your Results
Results from this test will be interpreted by qualified healthcare professionals. They will explain the significance of any identified genetic variations and how they may relate to hearing loss. A genetic counseling session is recommended to discuss results and implications further.
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, making it convenient for you to access our services. Additionally, we offer home sample collection services to ensure you can take the test with ease. Book your test today by calling or WhatsApp us at +254711564616!
Test Details
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Turnaround Time: 3 to 4 Weeks
- Pre-Test Instructions: A clinical history of the patient who is going for CATSPER2 Gene Deafness and male infertility, including a genetic counseling session to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness.
- Specialty: ENT Doctor
- Department: Genetics
- Method: NGS Technology
- Disease Type: Ear Nose Throat Disorders