Myo15A Gene Deafness Autosomal Recessive Type 3 NGS Genetic DNA Test
Introduction
The Myo15A Gene Deafness Autosomal Recessive Type 3 NGS Genetic DNA Test is a revolutionary diagnostic tool designed to uncover genetic mutations associated with hearing loss. This test is particularly crucial for individuals with a family history of deafness, as it can provide insights into hereditary patterns and potential risks for future generations.
What the Test Measures
This genetic test employs Next-Generation Sequencing (NGS) technology to identify mutations in the MYO15A gene. These mutations are linked to autosomal recessive deafness, allowing for a precise understanding of a patient’s genetic predisposition to hearing impairment.
Who Should Consider This Test
Individuals who should consider the Myo15A Gene Deafness Test include:
- Persons with a family history of hearing loss.
- Individuals exhibiting symptoms of hearing impairment.
- Patients referred by ENT doctors for genetic evaluation.
Benefits of Taking the Test
Taking the Myo15A Gene Deafness Test offers several benefits:
- Identification of genetic factors contributing to hearing loss.
- Informed family planning and risk assessment for future children.
- Guidance for treatment options and interventions.
- Access to genetic counseling for better understanding of results.
Understanding Your Results
Results from the Myo15A Gene Deafness Test will provide insights into whether mutations are present in the MYO15A gene. A genetic counselor will help interpret these results, explaining their implications for your health and family.
Test Information and Pricing
| Test Name | Regular Price (NGN) | Discount Price (NGN) |
|---|---|---|
| Myo15A Gene Deafness Autosomal Recessive Type 3 NGS Genetic DNA Test | 560,000 NGN | 400,000 NGN |
Booking the Test
To book the Myo15A Gene Deafness Autosomal Recessive Type 3 NGS Genetic DNA Test, contact us at +2348077798758. Our team is ready to assist you with any inquiries and scheduling.
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 test is required along with a genetic counseling session to draw a pedigree chart of family members affected by the MYO15A gene.
