TIMM8A Gene Jensen Syndrome Genetic Test
At DNA Labs UAE, we offer the TIMM8A Gene Jensen Syndrome Genetic Test to diagnose and identify the cost of this condition. Jensen syndrome, also known as Mohr-Tranebjaerg syndrome or X-linked deafness-dystonia syndrome, is a genetic disorder characterized by progressive hearing loss, movement disorders (such as dystonia), and cognitive decline.
Test Details
Our TIMM8A Gene Jensen Syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously. By sequencing the DNA of an individual and comparing it to a reference genome, we can identify any variations or mutations in the TIMM8A gene that may be responsible for the disorder.
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: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
Pre Test Information
Prior to undergoing the TIMM8A Gene Jensen Syndrome Genetic Test, it is recommended 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 by TIMM8A Gene Jensen Syndrome.
Consultation and Testing Process
If you suspect that you or someone you know may have Jensen syndrome, we advise consulting with a genetic counselor or healthcare provider. They can help determine if NGS genetic testing is appropriate and guide you through the testing process.
For more information or to schedule an appointment, please contact DNA Labs UAE.
Test Name | TIMM8A Gene Jensen syndrome Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Neurological Disorders |
Doctor | Neurologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for TIMM8A Gene Jensen syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TIMM8A Gene Jensen syndrome |
Test Details | The TIMM8A gene is associated with a condition called Jensen syndrome, also known as Mohr-Tranebjaerg syndrome or X-linked deafness-dystonia syndrome. This genetic disorder is characterized by progressive hearing loss, movement disorders (such as dystonia), and cognitive decline. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify any variations or mutations that may be associated with a particular condition. In the case of Jensen syndrome, NGS genetic testing can be used to identify variations or mutations in the TIMM8A gene that may be responsible for the disorder. NGS testing involves sequencing the DNA of an individual and comparing it to a reference genome to identify any differences. This allows for the detection of specific genetic changes that may be causing the symptoms of Jensen syndrome. If you suspect that you or someone you know may have Jensen syndrome, consulting with a genetic counselor or healthcare provider is recommended. They can help determine if NGS genetic testing is appropriate and guide you through the testing process. |