COL11A2 Gene Deafness Autosomal Recessive Type 53 Genetic Test
Are you concerned about your hearing? Do you suspect that you may have COL11A2 gene deafness autosomal recessive type 53 (DFNB53)? DNA Labs UAE offers a comprehensive genetic test that can provide answers.
Test Components
The COL11A2 Gene Deafness Autosomal Recessive Type 53 Genetic Test includes:
- NGS Technology
- Ear Nose Throat Disorders
- ENT Doctor
- Genetics Department
Price
The cost of the COL11A2 Gene Deafness Autosomal Recessive Type 53 Genetic Test is AED 4400.0.
Sample Condition
We accept the following sample conditions for testing:
- Blood
- Extracted DNA
- One drop of blood on FTA Card
Report Delivery
Once the sample is received, the report will be delivered within 3 to 4 weeks.
Method
We use NGS (Next-Generation Sequencing) technology for the COL11A2 Gene Deafness Autosomal Recessive Type 53 Genetic Test.
Test Type
The test is specifically designed to diagnose and analyze Ear Nose Throat Disorders.
Doctor
The test is conducted by an ENT Doctor who specializes in genetic testing.
Pre Test Information
Prior to the test, it is important to provide the clinical history of the patient. This is especially crucial for individuals who are going for the CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test. A Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test gene CATSPER10.
Test Details
The COL11A2 gene is associated with a type of deafness known as autosomal recessive type 53 (DFNB53). This means that individuals with two copies of a mutated COL11A2 gene will have this type of deafness.
NGS (Next-Generation Sequencing) genetic testing allows for the simultaneous sequencing of multiple genes or even the entire genome. In the case of COL11A2 gene deafness, NGS genetic testing can be used to identify mutations or variations in the COL11A2 gene that may be responsible for causing DFNB53.
The process involves extracting DNA from a patient’s sample (such as blood or saliva), sequencing the DNA using advanced sequencing technologies, and then analyzing the data to identify any mutations or variations in the COL11A2 gene.
By identifying mutations in the COL11A2 gene, NGS genetic testing can help diagnose individuals with DFNB53 and provide information about the genetic cause of their deafness. This can be valuable for understanding the inheritance pattern of the condition within a family and for making informed decisions regarding family planning or potential treatment options.
Test Name | COL11A2 Gene Deafness autosomal recessive type 53 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 CATSPER10 |
Test Details |
The COL11A2 gene is associated with a type of deafness known as autosomal recessive type 53 (DFNB53). This means that individuals with two copies of a mutated COL11A2 gene will have this type of deafness. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the case of COL11A2 gene deafness, NGS genetic testing can be used to identify mutations or variations in the COL11A2 gene that may be responsible for causing DFNB53. NGS genetic testing involves extracting DNA from a patient’s sample (such as blood or saliva), sequencing the DNA using advanced sequencing technologies, and then analyzing the data to identify any mutations or variations in the COL11A2 gene. By identifying mutations in the COL11A2 gene, NGS genetic testing can help diagnose individuals with DFNB53 and provide information about the genetic cause of their deafness. This can be valuable for understanding the inheritance pattern of the condition within a family and for making informed decisions regarding family planning or potential treatment options. |