Syne4 Gene Deafness Autosomal Recessive Type 76 NGS Genetic DNA Test
Introduction
The Syne4 Gene Deafness Autosomal Recessive Type 76 NGS Genetic DNA Test is a vital diagnostic tool that aids in identifying genetic mutations associated with deafness. This test utilizes Next-Generation Sequencing (NGS) technology to provide accurate results, helping patients and healthcare providers make informed decisions regarding treatment and management of hearing loss. Understanding your genetic makeup is essential, especially for those with a family history of hearing disorders.
What the Test Measures
This test specifically measures mutations in the SYNE4 gene, which have been linked to autosomal recessive deafness. By analyzing the genetic material, the test can detect variations that may predispose an individual to hearing loss.
Who Should Consider This Test?
Individuals who should consider the Syne4 Gene Deafness Test include:
- Those with a family history of deafness or hearing loss.
- Individuals experiencing unexplained hearing difficulties.
- Patients with symptoms such as tinnitus or progressive hearing loss.
Benefits of Taking the Test
Taking the Syne4 Gene Deafness Test offers several benefits, including:
- Early identification of genetic predispositions to hearing loss.
- Informed decision-making regarding potential interventions.
- Access to genetic counseling and resources for affected families.
Understanding Your Results
Results from the Syne4 Gene Deafness Test will be provided in a comprehensive report. It is essential to discuss these results with a healthcare professional who can explain the implications, potential risks, and options for management or treatment based on your genetic profile.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today
Don’t wait to understand your genetic health. Book the Syne4 Gene Deafness Autosomal Recessive Type 76 NGS Genetic DNA Test today! For inquiries or to schedule your appointment, please call or WhatsApp us at +2348077798758. Our dedicated team is here to assist you with all your diagnostic needs.
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 SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test. A genetic counseling session to draw a pedigree chart of family members affected with SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test gene SLC52A13.
This test is performed under the specialty of ENT doctors within the Genetics department, ensuring a comprehensive approach to ear, nose, and throat disorders.
