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TBC1D24 Gene Deafness Autosomal Recessive Type 86 Genetic Test Cost

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

-21%

The TBC1D24 gene is associated with a form of deafness known as Autosomal Recessive Deafness Type 86 (DFNB86). This condition is characterized by a genetic mutation in the TBC1D24 gene, leading to hearing impairment. The inheritance pattern of this condition is autosomal recessive, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected by the condition.

To diagnose this specific type of genetic deafness, a specialized genetic test is available at DNA Labs UAE. This test involves analyzing the DNA to identify mutations in the TBC1D24 gene that are responsible for the condition. It is a crucial step for families with a history of hearing loss or for individuals who have early signs of hearing impairment, providing them with essential information for making informed decisions about their health or family planning.

The cost of the TBC1D24 Gene Deafness Autosomal Recessive Type 86 Genetic Test at DNA Labs UAE is 4400 AED. The test is conducted with high precision and accuracy, ensuring reliable results for those being tested. After the test, genetic counseling may be recommended to discuss the results and understand the implications for the individual and their family.

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TBC1D24 Gene Deafness Autosomal Recessive Type 86 Genetic Test

At DNA Labs UAE, we offer the TBC1D24 Gene Deafness Autosomal Recessive Type 86 Genetic Test. This test helps in diagnosing and understanding the symptoms of DFNB86, a type of deafness associated with the TBC1D24 gene.

Test Components

  • Price: 4400.0 AED

Sample Condition

We accept blood samples, extracted DNA samples, or one drop of blood on an FTA card for this test.

Report Delivery

The test results will be delivered within 3 to 4 weeks.

Method

We use NGS (Next-Generation Sequencing) technology for this genetic test.

Test Type

This test is specifically designed for Ear Nose Throat Disorders.

Doctor

Our ENT Doctor specializes in conducting this test.

Test Department

This test falls under the Genetics department.

Pre Test Information

Prior to conducting the CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test, a Genetic Counselling session is recommended. This session helps in drawing a pedigree chart of family members affected by CATSPER2 Gene Deafness and male infertility. The gene CATSPER12 is also tested in this process.

Test Details

The TBC1D24 gene is associated with autosomal recessive type 86 (DFNB86) deafness. This means that an individual must inherit two copies of the mutated gene, one from each parent, to develop the condition. Our NGS genetic testing method analyzes the DNA sequence of an individual’s genes, allowing us to detect mutations or changes in the TBC1D24 gene that may be associated with DFNB86. This test provides valuable information about the risk of developing deafness, and it can assist with diagnosis, treatment, and genetic counseling.

It is important to consult with a healthcare professional or genetic counselor to determine if NGS genetic testing for the TBC1D24 gene is appropriate for you or your family members. They can provide personalized guidance and interpretation of the test results.

Test Name TBC1D24 Gene Deafness autosomal recessive type 86 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 CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test gene CATSPER12
Test Details

The TBC1D24 gene is associated with a type of deafness known as autosomal recessive type 86 (DFNB86). Autosomal recessive inheritance 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) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the detection of mutations or changes in the TBC1D24 gene that may be associated with DFNB86. This type of genetic testing can provide valuable information about an individual’s risk of developing deafness and can help with diagnosis, treatment, and genetic counseling.

It is important to consult with a healthcare professional or genetic counselor to determine if NGS genetic testing for the TBC1D24 gene is appropriate for you or your family members, as they can provide personalized guidance and interpretation of the test results.

SKU: TEST-2739 Category:

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