TRMU Gene Mitochondrial Modifier of Deafness NGS Genetic DNA Test
Introduction to the Test
The TRMU Gene Mitochondrial Modifier of Deafness NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with hearing loss. This test is crucial for individuals with a family history of deafness, providing insights into potential genetic risks that may contribute to this condition. By utilizing Next-Generation Sequencing (NGS) technology, the test offers a comprehensive analysis of the TRMU gene, enabling healthcare providers to deliver targeted interventions.
What the Test Measures
This genetic test specifically measures mutations in the TRMU gene, which plays a vital role in mitochondrial function and has been linked to various types of hearing loss. By detecting these mutations, the test can help in understanding the underlying genetic causes of deafness.
Who Should Consider This Test?
Individuals with the following conditions should consider the TRMU Gene Mitochondrial Modifier of Deafness NGS Genetic DNA Test:
- Family history of hearing loss or deafness
- Symptoms of hearing impairment
- Individuals undergoing infertility treatments, particularly males with suspected genetic contributions
Benefits of Taking the Test
The benefits of the TRMU Gene Mitochondrial Modifier of Deafness NGS Genetic DNA Test include:
- Early identification of genetic predispositions to hearing loss
- Informed family planning decisions
- Guidance for treatment options based on genetic findings
- Access to genetic counseling for better understanding and support
Understanding Your Results
Upon completion of the test, results will be interpreted by a qualified genetic specialist. They will provide a detailed report explaining any identified mutations and their implications for your health. This understanding can play a critical role in managing your health and making informed decisions.
Test Details and Pricing
| Test Name | TRMU Gene Mitochondrial Modifier of Deafness NGS Genetic DNA Test |
|---|---|
| Discount Price | 400000 NGN |
| Regular Price | 560000 NGN |
Booking Information
To book the TRMU Gene Mitochondrial Modifier of Deafness NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with any questions and ensure a seamless testing experience.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One Drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient undergoing the CATSPER2 Gene Deafness and male infertility test is required. A genetic counseling session is recommended to draw a pedigree chart of family members affected by CATSPER2 Gene Deafness and male infertility.
This test is performed under the supervision of ENT doctors and specialists in the Genetics department, ensuring that you receive the highest level of care and expertise.
