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TMPRSS3 Gene Deafness Autosomal Recessive Type 810 Genetic Test

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

-21%

The TMPRSS3 Gene Deafness Autosomal Recessive Type 810 Genetic Test is a specialized diagnostic examination aimed at identifying mutations in the TMPRSS3 gene, which are known to cause autosomal recessive nonsyndromic hearing loss. This condition, characterized by the absence of other accompanying symptoms, leads to varying degrees of hearing impairment from birth or early childhood. The TMPRSS3 gene plays a crucial role in the development and function of the inner ear, and mutations in this gene can disrupt normal hearing processes.

Conducted at DNA Labs UAE, a leading facility in genetic testing, this test is essential for families with a history of hearing loss, providing crucial information for early intervention and management strategies. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed for specific mutations in the TMPRSS3 gene.

The cost of the TMPRSS3 Gene Deafness Autosomal Recessive Type 810 Genetic Test is 4400 AED. This investment is significant for affected individuals and their families, as a positive identification of a mutation can lead to a better understanding of the condition, informed decision-making regarding treatment options, and the opportunity for genetic counseling regarding the risk of passing the condition to future generations.

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TMPRSS3 Gene Deafness Autosomal Recessive Type 810 Genetic Test

Welcome to DNA Labs UAE, where we offer the TMPRSS3 Gene Deafness Autosomal Recessive Type 810 Genetic Test. This test is designed to diagnose individuals with autosomal recessive type 8/10 deafness and provide valuable information about the specific genetic variant causing the condition.

Test Components and Price

The TMPRSS3 Gene Deafness Autosomal Recessive Type 810 Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Method and Test Type

The TMPRSS3 Gene Deafness Autosomal Recessive Type 810 Genetic Test utilizes NGS (Next-Generation Sequencing) technology. This advanced genetic testing method allows for the sequencing of multiple genes simultaneously. The test specifically focuses on genes related to Ear Nose Throat Disorders.

Doctor and Test Department

The test is conducted under the supervision of an ENT Doctor in our Genetics department.

Pre-Test Information

Prior to undergoing the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN33.

Test Details

The TMPRSS3 gene is associated with deafness, specifically autosomal recessive type 8/10. Autosomal recessive means that an individual must inherit two copies of the mutated gene (one from each parent) in order to develop the condition. The NGS genetic test involves sequencing the TMPRSS3 gene to identify any mutations or variations associated with the condition. This test is not only helpful in diagnosing individuals with autosomal recessive type 8/10 deafness, but it can also provide information about the specific genetic variant causing the condition. It can also be used for carrier testing in individuals with a family history of TMPRSS3-related deafness. By identifying carriers, we can provide valuable information for genetic counseling and potentially guide treatment options in the future.

Test Name TMPRSS3 Gene Deafness autosomal recessive type 810 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 PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN33
Test Details

The TMPRSS3 gene is associated with deafness, specifically autosomal recessive type 8/10. Autosomal recessive means that an individual must inherit two copies of the mutated gene (one from each parent) in order to develop the condition.

NGS (Next-Generation Sequencing) is a type of genetic test that allows for the sequencing of multiple genes simultaneously. In the context of TMPRSS3 gene deafness, an NGS genetic test would involve sequencing the TMPRSS3 gene to identify any mutations or variations that may be associated with the condition.

This genetic test can help diagnose individuals with autosomal recessive type 8/10 deafness and provide information about the specific genetic variant causing the condition. It can also be used for carrier testing in individuals with a family history of TMPRSS3-related deafness, as carriers have one normal and one mutated copy of the gene.

Overall, the TMPRSS3 gene NGS genetic test can provide valuable information for individuals and families affected by autosomal recessive type 8/10 deafness, aiding in diagnosis, genetic counseling, and potentially guiding treatment options in the future.

SKU: TEST-2738 Category:

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