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GJB3 Gene Deafness Autosomal Dominant Type 2B Genetic Test Cost

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

-21%

The GJB3 Gene Deafness Autosomal Dominant Type 2B Genetic Test is a specialized diagnostic tool designed to identify mutations in the GJB3 gene, which have been linked to a form of hearing loss known as Autosomal Dominant Deafness Type 2B. This condition is characterized by varying degrees of hearing impairment, which can be present from birth or develop later in life. The test is crucial for individuals with a family history of hearing loss or those experiencing symptoms, as it can provide definitive genetic evidence of the condition, enabling early intervention and tailored management strategies.

Performed at DNA Labs UAE, the test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities in the GJB3 gene. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in this specific gene. By opting for this test, individuals gain valuable insights into their genetic makeup, empowering them with the information needed to make informed decisions about their health and the health of their families.

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GJB3 Gene Deafness autosomal dominant type 2B Genetic Test

Welcome to DNA Labs UAE, where we offer the GJB3 Gene Deafness autosomal dominant type 2B Genetic Test. In this blog, we will provide you with detailed information about the test, including its cost, symptoms, diagnosis, and more.

Test Details

The GJB3 gene deafness, autosomal dominant type 2B NGS genetic test is a type of genetic test that analyzes the GJB3 gene for mutations associated with autosomal dominant type 2B deafness. This test uses next-generation sequencing (NGS) technology to examine the DNA sequence of the GJB3 gene and identify any genetic variations or mutations that may be causing or contributing to the hearing loss.

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 GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test gene GJB4.

The GJB3 gene deafness, autosomal dominant type 2B NGS genetic test can help in the diagnosis of autosomal dominant type 2B deafness by identifying specific mutations or variations in the GJB3 gene. This information can be useful for genetic counseling, determining the inheritance pattern of the condition within a family, and potentially guiding treatment or management strategies.

It’s important to note that this genetic test is specific to GJB3 gene deafness and does not analyze other genes or conditions. Additionally, the test may not detect all possible mutations in the GJB3 gene, as there may be rare or novel variations that are not included in the test panel. Therefore, it’s always recommended to consult with a healthcare professional or genetic counselor to determine the most appropriate genetic test for an individual’s specific situation.

Thank you for choosing DNA Labs UAE for your genetic testing needs. If you have any further questions or would like to schedule an appointment, please don’t hesitate to contact us.

Test Name GJB3 Gene Deafness autosomal dominant type 2B 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 GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test gene GJB4
Test Details

GJB3 gene deafness, autosomal dominant type 2B NGS genetic test is a type of genetic test that analyzes the GJB3 gene for mutations associated with autosomal dominant type 2B deafness. This test uses next-generation sequencing (NGS) technology to examine the DNA sequence of the GJB3 gene and identify any genetic variations or mutations that may be causing or contributing to the hearing loss.

Autosomal dominant type 2B deafness is a genetic condition characterized by progressive hearing loss that typically begins in childhood or adolescence. Mutations in the GJB3 gene, which codes for a protein called connexin 31, are known to cause this type of deafness. The connexin 31 protein is involved in the formation of gap junctions in the inner ear, which are important for normal hearing.

The NGS genetic test for GJB3 gene deafness can help in the diagnosis of autosomal dominant type 2B deafness by identifying specific mutations or variations in the GJB3 gene. This information can be useful for genetic counseling, determining the inheritance pattern of the condition within a family, and potentially guiding treatment or management strategies.

It’s important to note that this genetic test is specific to GJB3 gene deafness and does not analyze other genes or conditions. Additionally, the test may not detect all possible mutations in the GJB3 gene, as there may be rare or novel variations that are not included in the test panel. Therefore, it’s always recommended to consult with a healthcare professional or genetic counselor to determine the most appropriate genetic test for an individual’s specific situation.

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