GJB6 Gene Deafness Autosomal Recessive Type 1B NGS Genetic DNA Test
Introduction
The GJB6 Gene Deafness Autosomal Recessive Type 1B NGS Genetic DNA Test is a cutting-edge diagnostic tool that leverages Next-Generation Sequencing (NGS) technology to identify genetic mutations associated with autosomal recessive deafness. This test is crucial for individuals with a family history of hearing loss or those experiencing unexplained hearing impairment.
What the Test Measures
This genetic test specifically measures mutations in the GJB6 gene, which is known to play a significant role in the development of auditory function. By detecting these mutations, healthcare providers can better understand the underlying causes of deafness in patients.
Who Should Consider This Test
Individuals who should consider the GJB6 Gene Deafness test include:
- Those with a family history of hearing loss.
- Individuals displaying symptoms of deafness.
- Patients with unexplained auditory issues.
Benefits of Taking the Test
Taking the GJB6 Gene Deafness test provides numerous benefits, including:
- Accurate identification of genetic causes of hearing loss.
- Guidance for family planning and genetic counseling.
- Informed decisions regarding treatment options.
- Enhanced understanding of personal health risks.
Understanding Your Results
Results from the GJB6 Gene Deafness test will indicate whether mutations are present in the GJB6 gene. A positive result may suggest a genetic predisposition to hearing loss, while a negative result can provide reassurance. It is essential to discuss your results with a healthcare professional 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 understand your genetic health. Book the GJB6 Gene Deafness Autosomal Recessive Type 1B NGS Genetic DNA Test today! For more information or to schedule your appointment, contact us at +2348077798758.
Turnaround time for results is approximately 3 to 4 weeks. The test requires a sample of blood, extracted DNA, or one drop of blood on an FTA card. Prior to the test, a clinical history and genetic counseling session are advised to discuss family members affected by hearing disorders.
