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 |
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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. |