PJVK Gene Deafness Autosomal Recessive Type 59 NGS Genetic DNA Test
Introduction to the Test
The PJVK Gene Deafness Autosomal Recessive Type 59 NGS Genetic DNA Test is a crucial diagnostic tool designed to assess genetic mutations associated with hearing loss. This test employs Next Generation Sequencing (NGS) technology to provide comprehensive insights into the genetic factors contributing to deafness, specifically focusing on the PJVK gene.
What the Test Measures
This genetic test measures specific mutations in the PJVK gene that are known to cause autosomal recessive hearing loss. By identifying these mutations, healthcare providers can better understand the underlying genetic causes of deafness in patients.
Who Should Consider This Test?
Individuals who should consider the PJVK Gene Deafness Test include:
- Those with a family history of deafness or hearing loss.
- Individuals exhibiting symptoms of hearing impairment.
- Patients with a clinical history suggestive of genetic hearing loss.
Benefits of Taking the Test
The benefits of undergoing the PJVK Gene Deafness Test include:
- Accurate diagnosis of genetic causes of hearing loss.
- Informed decision-making regarding treatment options.
- Potential for early intervention and management strategies.
- Understanding family planning options based on genetic findings.
Understanding Your Results
Results from the PJVK Gene Deafness Test will provide insights into whether specific genetic mutations are present. A genetic counselor will help interpret these results, explaining their implications for the patient and their family.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| PJVK Gene Deafness Autosomal Recessive Type 59 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To schedule your PJVK Gene Deafness Autosomal Recessive Type 59 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you in understanding the importance of this test and ensuring a smooth booking process.
Turnaround time for results is approximately 3 to 4 weeks. The test requires a sample type of blood or extracted DNA, or one drop of blood on an FTA card. Prior to the test, a clinical history and genetic counseling session is advised to draw a pedigree chart of affected family members.
Consult with an ENT doctor or a genetic specialist to determine if this test is right for you and your family.
