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MYO1A Gene Deafness Autosomal Dominant Type 48 Genetic Test Cost

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

-21%

The MYO1A Gene Deafness Autosomal Dominant Type 48 Genetic Test is a specialized diagnostic tool designed to identify mutations in the MYO1A gene, which are linked to Autosomal Dominant Non-Syndromic Hearing Loss (ADNSHL), specifically categorized as Type 48. This form of hearing loss is characterized by its genetic inheritance pattern, where a single copy of the altered gene in each cell is sufficient to cause the disorder. The MYO1A gene plays a crucial role in the development and maintenance of the inner ear’s structure, which is essential for proper hearing.

Conducted at DNA Labs UAE, this test aims to provide individuals and families with critical genetic information that can help in understanding the risk of developing this type of hearing loss or passing it on to future generations. Early detection through this genetic test can facilitate timely interventions and support measures to manage the condition effectively.

The cost of the MYO1A Gene Deafness Autosomal Dominant Type 48 Genetic Test is set at 4400 AED. This investment covers the comprehensive analysis required to detect mutations in the MYO1A gene, offering a valuable resource for affected individuals and their healthcare providers in devising personalized management plans and making informed decisions about their health and well-being.

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MYO1A Gene Deafness autosomal dominant type 48 Genetic Test

Welcome to DNA Labs UAE, where we offer the MYO1A Gene Deafness autosomal dominant type 48 Genetic Test. This test is designed to identify mutations in the MYO1A gene that are associated with deafness type 48 (DFNA48), a form of autosomal dominant deafness.

Test Components and Price

The MYO1A Gene Deafness autosomal dominant type 48 Genetic Test is priced at 4400.0 AED. The test requires a sample of either blood, extracted DNA, or one drop of blood on an FTA Card.

Report Delivery and Method

After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology, which allows for the sequencing of the entire coding region of the MYO1A gene.

Test Type and Doctor

The MYO1A Gene Deafness autosomal dominant type 48 Genetic Test falls under the category of Ear Nose Throat Disorders. It is recommended to consult with an ENT Doctor for this test.

Test Department and Pre Test Information

The MYO1A Gene Deafness autosomal dominant type 48 Genetic Test is conducted by our Genetics department. It is important to provide the clinical history of the patient who is going for the test, especially if they are affected with EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session may be required to draw a pedigree chart of family members affected with EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA5.

Test Details and Importance

The MYO1A gene is associated with autosomal dominant deafness, specifically known as deafness type 48 (DFNA48). Autosomal dominant means that only one copy of the mutated gene is needed to cause the condition. By performing an NGS genetic test on the MYO1A gene, individuals can determine if they carry a mutation associated with DFNA48. This information is crucial for diagnosis, genetic counseling, and potentially for guiding treatment options or management strategies.

Test Name MYO1A Gene Deafness autosomal dominant type 48 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 EYA5
Test Details

The MYO1A gene is associated with a form of autosomal dominant deafness, specifically known as deafness type 48 (DFNA48). Autosomal dominant means that only one copy of the mutated gene is needed to cause the condition.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. It allows for the sequencing of the entire coding region of the MYO1A gene to identify any mutations or variants that may be present.

By performing an NGS genetic test on the MYO1A gene, individuals can determine if they carry a mutation that is associated with DFNA48. This information can be useful for diagnosis, genetic counseling, and potentially for guiding treatment options or management strategies.

SKU: TEST-2692 Category:

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