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ESPN Gene Deafness Autosomal Recessive Type 36 Genetic Test

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

-21%

The “ESPN Gene Deafness Autosomal Recessive Type 36 Genetic Test” is a specific diagnostic tool designed to detect mutations in the ESPN gene, which can lead to autosomal recessive nonsyndromic deafness 36 (DFNB36). This condition is characterized by hearing loss that does not present with other symptoms. The test is crucial for early detection, allowing for timely intervention and management strategies to improve the quality of life for affected individuals.

Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities, the test involves analyzing the patient’s DNA to identify any alterations in the ESPN gene. These mutations disrupt the normal function of the protein produced by the gene, leading to the development of hearing loss.

The cost of the test is set at 4400 AED, reflecting the intricate process of genetic analysis and the specialized expertise required to interpret the results. By offering this test, DNA Labs UAE provides a vital resource for families with a history of hearing loss, enabling them to make informed decisions about their health and future.

Home  Sample collection service available

  • 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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ESPN Gene Deafness Autosomal Recessive Type 36 Genetic Test

At DNA Labs UAE, we offer the ESPN Gene Deafness Autosomal Recessive Type 36 Genetic Test at a cost of AED 4400.0.

Test Details

The ESPN gene is associated with autosomal recessive type 36 deafness. This means that in order to develop the condition, an individual must inherit two copies of the mutated gene, one from each parent. Our Next-Generation Sequencing (NGS) technology allows us to analyze multiple genes simultaneously and identify any mutations or variants in the ESPN gene that may be causing the condition.

NGS genetic testing is a valuable tool for diagnosis, genetic counseling, and potentially guiding treatment options. By identifying the specific genetic mutation causing deafness, we can provide important information for family members who may be at risk of carrying the mutated gene.

Test Components and Price

  • Components: ESPN Gene Deafness Autosomal Recessive Type 36 Genetic Test
  • Price: AED 4400.0

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on an FTA card for this test.

Report Delivery

Your test report will be delivered within 3 to 4 weeks.

Test Type and Department

  • Test Type: Ear Nose Throat Disorders
  • Test Department: Genetics

Doctor and Pre-Test Information

Our ENT doctor will oversee the ESPN Gene Deafness Autosomal Recessive Type 36 Genetic Test. Prior to the test, we recommend a genetic counseling session to draw a pedigree chart of family members affected with GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test gene GJB9.

During the session, we will gather clinical history of the patient who is going for the test. This information will help us provide a comprehensive analysis and interpretation of the test results.

Method

The ESPN Gene Deafness Autosomal Recessive Type 36 Genetic Test is conducted using NGS technology.

Conclusion

If you or your family members are experiencing symptoms of ESPN gene deafness, it is important to consult with a healthcare professional or genetic counselor. Our ESPN Gene Deafness Autosomal Recessive Type 36 Genetic Test can provide valuable insights for diagnosis, genetic counseling, and potential treatment options.

Test Name ESPN Gene Deafness autosomal recessive 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 GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test gene GJB9
Test Details

The ESPN gene is associated with autosomal recessive type 36 deafness. Autosomal recessive inheritance means that an individual must inherit two copies of the mutated gene (one from each parent) in order to develop the condition.

NGS (Next-Generation Sequencing) is a type of genetic testing that can analyze multiple genes simultaneously to identify any mutations or variants that may be present. In the case of ESPN gene deafness, an NGS genetic test can be used to identify any mutations or variants in the ESPN gene that may be causing the condition.

By identifying the specific genetic mutation causing deafness, NGS testing can help with diagnosis, genetic counseling, and potentially guide treatment options. It can also provide valuable information for family members who may be at risk of carrying the mutated gene.

It is important to consult with a healthcare professional or genetic counselor for further information and guidance regarding ESPN gene deafness and NGS genetic testing.