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GJB6 Gene Deafness Autosomal Recessive Type 1B Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The GJB6 gene, also known as Gap Junction Beta 6, plays a crucial role in the development and function of the cochlea, the auditory portion of the inner ear. Mutations in this gene are associated with a form of non-syndromic hearing loss, specifically autosomal recessive deafness type 1B. This condition is characterized by the inheritance of two copies of the mutated gene, one from each parent, leading to a higher risk of developing hearing loss from birth or early childhood without affecting other body systems.

To diagnose this condition, a genetic test targeting the GJB6 gene can be conducted. This test involves analyzing the patient’s DNA to identify mutations in the GJB6 gene that are known to cause deafness. The test is particularly useful for families with a history of hearing loss and can provide valuable information for early intervention and management strategies for affected individuals.

In the UAE, DNA Labs offers this specialized genetic test for identifying mutations in the GJB6 gene associated with autosomal recessive deafness type 1B. The cost of the test is set at 4400 AED. Conducting the test at DNA Labs UAE ensures that patients receive accurate and reliable results, thanks to the lab’s state-of-the-art technology and expertise in genetic diagnostics. Early detection through this test can significantly impact the quality of life of individuals with hereditary deafness, allowing for timely interventions such as hearing aids, cochlear implants, or other supportive measures to enhance hearing and communication skills.

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GJB6 Gene Deafness autosomal recessive type 1B Genetic Test

Welcome to DNA Labs UAE, where we offer the GJB6 Gene Deafness autosomal recessive type 1B Genetic Test. This test is designed to diagnose and provide valuable insights into the condition known as Deafness, autosomal recessive type 1B (DFNB1B).

Test Details

The GJB6 gene is responsible for producing a protein called connexin 30, which plays a crucial role in the formation of gap junctions in the inner ear. Gap junctions are channels that allow the exchange of ions and small molecules between cells, which is essential for the normal functioning of the auditory system.

DFNB1B is a genetic condition characterized by moderate to profound hearing loss. It is caused by mutations in the GJB6 gene, resulting in a loss or dysfunction of connexin 30. Our Next-Generation Sequencing (NGS) technology allows for the simultaneous analysis of multiple genes, including GJB6, in a single test. This enables the identification of various mutations and genetic variants associated with DFNB1B.

Test Components and Price

Our GJB6 Gene Deafness autosomal recessive type 1B Genetic Test is priced at AED 4400.0. The test can be conducted using a blood sample, extracted DNA, or even just one drop of blood on an FTA Card.

Report Delivery and Method

Once the test is conducted, the report will be delivered within 3 to 4 weeks. Our NGS technology ensures accurate and efficient analysis of the genetic information.

Test Type and Doctor

The GJB6 Gene Deafness autosomal recessive type 1B Genetic Test falls under the category of Ear Nose Throat Disorders. It is recommended to consult with an ENT Doctor for this test.

Test Department and Pre-Test Information

The GJB6 Gene Deafness autosomal recessive type 1B Genetic Test is conducted in our Genetics department. Before taking the test, it is important to provide the clinical history of the patient who is going for the SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test. A Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test gene SLC52A9.

Benefits of the GJB6 Gene Deafness autosomal recessive type 1B Genetic Test

By performing an NGS genetic test for GJB6 gene mutations, individuals with suspected DFNB1B can receive a definitive diagnosis. This information can help guide treatment options and provide valuable insights into the inheritance pattern and recurrence risk for affected individuals and their families.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to schedule your GJB6 Gene Deafness autosomal recessive type 1B Genetic Test.

Test Name GJB6 Gene Deafness autosomal recessive type 1B Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Ear Nose Throat Disorders
Doctor ENT Doctor
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test gene SLC52A9
Test Details

The GJB6 gene is responsible for producing a protein called connexin 30, which is involved in the formation of gap junctions in the inner ear. Gap junctions are channels that allow the exchange of ions and small molecules between cells, which is crucial for the normal functioning of the auditory system.

Deafness, autosomal recessive type 1B (DFNB1B) is a genetic condition characterized by moderate to profound hearing loss. It is caused by mutations in the GJB6 gene, resulting in a loss or dysfunction of connexin 30.

NGS (Next-Generation Sequencing) is a high-throughput genetic testing method that allows for the simultaneous analysis of multiple genes, including GJB6, in a single test. This technology enables the identification of various mutations and genetic variants associated with DFNB1B.

By performing an NGS genetic test for GJB6 gene mutations, individuals with suspected DFNB1B can receive a definitive diagnosis. This information can help guide treatment options and provide valuable insights into the inheritance pattern and recurrence risk for affected individuals and their families.

SKU: TEST-2707 Category:

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