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TMC1 Gene Deafness Autosomal Dominant Type 36 Genetic Test Cost

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

-21%

The TMC1 Gene Deafness Autosomal Dominant Type 36 Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to detect mutations in the TMC1 gene, which are associated with Autosomal Dominant Non-Syndromic Hearing Loss (ADNSHL) type 36. This condition is characterized by varying degrees of hearing impairment that can present from birth or develop later in life, primarily affecting the ability to perceive sound due to genetic abnormalities.

This test is crucial for individuals with a family history of hearing loss or those showing symptoms of auditory impairment, as it helps in confirming the diagnosis, understanding the risk of transmission to offspring, and aiding in the management and treatment planning of the condition. By analyzing a sample of the patient’s DNA, the test identifies specific mutations in the TMC1 gene that are linked to this form of hearing loss, providing valuable genetic insights.

The cost of the TMC1 Gene Deafness Autosomal Dominant Type 36 Genetic Test at DNA Labs UAE is 4400 AED. The price reflects the comprehensive nature of the genetic analysis, the expertise required to interpret the results, and the significant impact the findings can have on the patient’s treatment and lifestyle adjustments. Patients considering this test are advised to consult with a healthcare provider or a genetic counselor to understand its implications fully and how the results may influence their health management strategies.

Description

TMC1 Gene Deafness Autosomal Dominant Type 36 Genetic Test

Test Name: TMC1 Gene Deafness Autosomal Dominant Type 36 Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Ear Nose Throat Disorders

Doctor: ENT Doctor

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA4

Test Details: TMC1 gene deafness, autosomal dominant type 36 is a specific type of genetic hearing loss caused by mutations in the TMC1 gene. This gene provides instructions for making a protein that is important for the normal functioning of hair cells in the inner ear, which are responsible for converting sound vibrations into electrical signals that can be interpreted by the brain.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of TMC1 gene deafness, autosomal dominant type 36, NGS genetic testing can identify any mutations or variations in the TMC1 gene that may be responsible for the hearing loss. This type of genetic test can help diagnose individuals with TMC1 gene deafness, autosomal dominant type 36, and can also be used for carrier testing in individuals with a family history of the condition. It can provide valuable information for genetic counseling, family planning, and potentially guide treatment options for individuals with this type of genetic hearing loss.

Test Name	TMC1 Gene Deafness autosomal dominant type 36 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 EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA4
Test Details	TMC1 gene deafness, autosomal dominant type 36 is a specific type of genetic hearing loss caused by mutations in the TMC1 gene. This gene provides instructions for making a protein that is important for the normal functioning of hair cells in the inner ear, which are responsible for converting sound vibrations into electrical signals that can be interpreted by the brain. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of TMC1 gene deafness, autosomal dominant type 36, NGS genetic testing can identify any mutations or variations in the TMC1 gene that may be responsible for the hearing loss. This type of genetic test can help diagnose individuals with TMC1 gene deafness, autosomal dominant type 36, and can also be used for carrier testing in individuals with a family history of the condition. It can provide valuable information for genetic counseling, family planning, and potentially guide treatment options for individuals with this type of genetic hearing loss.