GJB2 Gene Deafness Autosomal Recessive Type 1A NGS Genetic DNA Test
Introduction to the Test
The GJB2 Gene Deafness Autosomal Recessive Type 1A NGS Genetic DNA Test is a sophisticated diagnostic tool designed to identify genetic mutations in the GJB2 gene, a common cause of autosomal recessive hearing loss. This test employs Next Generation Sequencing (NGS) technology, allowing for precise detection of genetic abnormalities that may contribute to hearing impairment.
What the Test Measures
This test specifically measures the presence of mutations in the GJB2 gene. By analyzing the genetic code, it can detect changes that may lead to hearing loss, providing valuable insights into the underlying causes of auditory disorders.
Who Should Consider This Test?
Individuals who should consider the GJB2 Gene Deafness Test include:
- Those with a family history of hearing loss.
- Patients exhibiting symptoms of hearing impairment.
- Individuals seeking genetic counseling for hereditary hearing disorders.
Benefits of Taking the Test
- Accurate diagnosis of genetic hearing loss.
- Informed decision-making regarding treatment options.
- Guidance for family planning and genetic counseling.
- Understanding the risk of hearing loss in family members.
Understanding Your Results
Results from the GJB2 Gene Deafness Test will be interpreted by qualified genetic counselors or ENT specialists. A positive result indicates the presence of a mutation associated with hearing loss, while a negative result suggests that no such mutations were detected. It is essential to discuss your results with your healthcare provider to understand their implications fully.
Test Pricing
Price Type | Amount (NGN) |
---|---|
Discount Price | 400,000 NGN |
Regular Price | 560,000 NGN |
Book Your Test Today!
Don’t wait to gain clarity on your hearing health. To book the GJB2 Gene Deafness Autosomal Recessive Type 1A NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our team is ready to assist you in scheduling your appointment and answering any questions you may have.
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 going for the EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test is required. A genetic counseling session to draw a pedigree chart of family members affected with EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA7 is also necessary.
Consult with an ENT doctor or a genetic specialist for more information regarding this test and its implications on your health.