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WHRN Gene Deafness Autosomal Recessive Type 31 Genetic Test

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

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The WHRN gene, also known as whirlin, is linked to a type of hearing loss known as Deafness Autosomal Recessive Type 31 (DFNB31). This genetic condition is characterized by the mutation in the WHRN gene, which plays a crucial role in the development and maintenance of the inner ear’s structure and function. Individuals with mutations in this gene typically experience prelingual, non-syndromic sensorineural hearing loss, meaning the hearing loss occurs before speech development and is not associated with other symptoms.

To diagnose this specific genetic form of deafness, a genetic test is available at DNA Labs UAE. The test specifically looks for mutations in the WHRN gene that are known to cause DFNB31. It involves collecting a DNA sample, usually through a blood draw or a cheek swab, and then analyzing the genetic material for the presence of mutations.

The cost of the WHRN Gene Deafness Autosomal Recessive Type 31 Genetic Test at DNA Labs UAE is 4400 AED. This test is crucial for families with a history of this type of hearing loss, as it can provide a definitive diagnosis, guide treatment options, and offer information on the risk of passing the condition to future generations.

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WHRN Gene Deafness Autosomal Recessive Type 31 Genetic Test

At DNA Labs UAE, we offer the WHRN Gene Deafness Autosomal Recessive Type 31 Genetic Test. This test is designed to detect mutations in the WHRN gene that are associated with deafness, specifically autosomal recessive type 31 (DFNB31).

Test Details

The WHRN gene is responsible for causing deafness in individuals who have inherited two copies of the mutated gene, one from each parent. Our NGS (Next-Generation Sequencing) genetic testing method allows us to analyze multiple genes simultaneously, including the WHRN gene.

By performing this test, individuals with a suspected or known family history of autosomal recessive type 31 deafness can determine if they carry mutations in the WHRN gene. This information can be valuable for genetic counseling, family planning, and potentially identifying treatment options or interventions for managing the condition.

Test Components and Price

The WHRN Gene Deafness Autosomal Recessive Type 31 Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

After the sample is received, the report will be delivered within 3 to 4 weeks.

Test Type and Doctor

The WHRN Gene Deafness Autosomal Recessive Type 31 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 WHRN Gene Deafness Autosomal Recessive Type 31 Genetic Test is conducted in our Genetics department. Before undergoing the test, it is important to provide the clinical history of the patient who is going for the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session may also be conducted to draw a pedigree chart of family members affected with the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN30.

For more information or to schedule an appointment for the WHRN Gene Deafness Autosomal Recessive Type 31 Genetic Test, please contact DNA Labs UAE.

Test Name WHRN Gene Deafness autosomal recessive type 31 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 PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN30
Test Details

The WHRN gene is associated with deafness, specifically autosomal recessive type 31 (DFNB31). Autosomal recessive means that an individual must inherit two copies of the mutated gene, one from each parent, to develop the condition.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the case of WHRN gene deafness, NGS genetic testing can identify mutations or variations in the WHRN gene that may be responsible for causing deafness.

By performing this test, individuals with a suspected or known family history of autosomal recessive type 31 deafness can determine if they carry mutations in the WHRN gene. This information can be useful for genetic counseling, family planning, and potentially identifying treatment options or interventions for managing the condition.

SKU: TEST-2717 Category:

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