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TIMM8A Gene Jensen Syndrome Genetic Test

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

-21%

The TIMM8A Gene Jensen Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the TIMM8A gene, which are associated with Jensen Syndrome. This rare genetic disorder is characterized by deafness, dystonia (a movement disorder), and visual impairment, among other symptoms. The test plays a crucial role in confirming the diagnosis, allowing for early intervention and management strategies to be implemented.

Priced at 4400 AED, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific mutations in the TIMM8A gene. The results can provide valuable information for affected individuals and their families, including insights into the risk of passing the condition to future generations.

DNA Labs UAE is equipped with state-of-the-art technology and staffed by genetic experts, ensuring high accuracy and reliability of the test results. By opting for the TIMM8A Gene Jensen Syndrome Genetic Test, patients and healthcare providers can make informed decisions about treatment options and care plans, improving the quality of life for those affected by the syndrome.

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  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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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.