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TIMM8A Gene Dystonia-Deafness Syndrome Genetic Test Cost

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

-21%

The TIMM8A gene dystonia-deafness syndrome, also known as Mohr-Tranebjaerg syndrome, is a rare genetic disorder characterized by progressive hearing loss, dystonia, visual impairment, and neurological decline. The condition is inherited in an X-linked recessive pattern, affecting primarily males, though female carriers may exhibit some symptoms.

To diagnose this condition, a specific genetic test targeting the TIMM8A gene can be conducted. DNA Labs UAE offers this specialized test, designed to detect mutations in the TIMM8A gene that are responsible for the syndrome. The test is crucial for accurate diagnosis, enabling early intervention and management strategies to alleviate symptoms and improve quality of life for affected individuals.

The cost of the TIMM8A gene dystonia-deafness syndrome genetic test at DNA Labs UAE is 4400 AED. This price includes the genetic analysis and a comprehensive report, which provides detailed insights into the individual’s genetic makeup concerning the TIMM8A gene. The test is conducted with a high level of accuracy, using advanced genomic technologies to ensure reliable results. Families with a history of the syndrome or individuals showing symptoms are encouraged to consider this test for a definitive diagnosis and to inform potential treatment paths.

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TIMM8A Gene Dystonia-deafness syndrome Genetic Test

Test Name: TIMM8A Gene Dystonia-deafness syndrome Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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: Clinical History of Patient who is going for TIMM8A Gene Dystonia-deafness syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TIMM8A Gene Dystonia-deafness syndrome.

Test Details

The TIMM8A gene is responsible for producing a protein that plays a crucial role in the functioning of the inner ear and brain. Mutations in this gene can cause a rare genetic disorder called dystonia-deafness syndrome, which is characterized by a combination of hearing loss and involuntary muscle contractions or spasms (dystonia).

NGS (next-generation sequencing) genetic testing can be used to analyze the DNA sequence of the TIMM8A gene and identify any mutations that may be present. This type of testing can provide a definitive diagnosis for individuals with suspected dystonia-deafness syndrome, allowing for early intervention and management of symptoms.

NGS testing can also be used to identify carriers of the TIMM8A gene mutation, which can be important for family planning and genetic counseling.

Overall, NGS genetic testing for dystonia-deafness syndrome can provide valuable information for individuals and families affected by this rare genetic disorder.

Test Name TIMM8A Gene Dystonia-deafness 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 Dystonia-deafness syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TIMM8A Gene Dystonia-deafness syndrome
Test Details

The TIMM8A gene is responsible for producing a protein that plays a crucial role in the functioning of the inner ear and brain. Mutations in this gene can cause a rare genetic disorder called dystonia-deafness syndrome, which is characterized by a combination of hearing loss and involuntary muscle contractions or spasms (dystonia).

NGS (next-generation sequencing) genetic testing can be used to analyze the DNA sequence of the TIMM8A gene and identify any mutations that may be present. This type of testing can provide a definitive diagnosis for individuals with suspected dystonia-deafness syndrome, allowing for early intervention and management of symptoms.

NGS testing can also be used to identify carriers of the TIMM8A gene mutation, which can be important for family planning and genetic counseling. Overall, NGS genetic testing for dystonia-deafness syndrome can provide valuable information for individuals and families affected by this rare genetic disorder.

SKU: TEST-1257 Category:

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