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GRXCR1 Gene Deafness Autosomal Recessive Type 25 Genetic Test Cost

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

-21%

The GRXCR1 gene is associated with a form of hereditary hearing loss known as deafness, autosomal recessive type 25 (DFNB25). This condition is characterized by a range of hearing impairments, from mild to profound, that are present from birth. The GRXCR1 gene plays a crucial role in the development and maintenance of hair cells within the inner ear, which are essential for normal hearing function.

At DNA Labs UAE, individuals concerned about their risk of inheriting or passing on this form of deafness can undergo a genetic test specifically designed to identify mutations in the GRXCR1 gene. The test is conducted through a simple and non-invasive procedure, typically involving a blood sample or cheek swab, which is then analyzed in the laboratory to detect any genetic anomalies associated with DFNB25.

The cost of the GRXCR1 gene deafness autosomal recessive type 25 genetic test at DNA Labs UAE is 4400 AED. This investment provides valuable insights into an individual’s genetic predisposition to this form of hearing loss, enabling early intervention and informed decision-making regarding family planning. It is a critical resource for families with a history of hearing impairment, offering a path to better understand their genetic health and the potential for future generations.

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GRXCR1 Gene Deafness Autosomal Recessive Type 25 Genetic Test

Are you or someone you know experiencing deafness? DNA Labs UAE offers the GRXCR1 Gene Deafness Autosomal Recessive Type 25 Genetic Test to help diagnose individuals with this specific form of deafness. Read on to learn more about this test.

Test Details

The GRXCR1 gene is associated with deafness, specifically autosomal recessive type 25 (DFNB25). Autosomal recessive inheritance means that an individual needs to inherit two copies of the mutated gene, one from each parent, in order to develop the condition.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that analyzes multiple genes simultaneously. It uses high-throughput sequencing technology to efficiently sequence large amounts of DNA and identify genetic variations, such as mutations or changes, in the genes being analyzed.

In the context of GRXCR1 gene deafness, an NGS genetic test would involve sequencing the GRXCR1 gene to identify any variations or mutations that may be associated with autosomal recessive type 25 deafness. This test can help diagnose individuals with this specific form of deafness and provide important information for genetic counseling and management of the condition.

Test Components

  • Test Name: GRXCR1 Gene Deafness Autosomal Recessive Type 25 Genetic Test
  • 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

If you are considering this test, it is important to provide the clinical history of the patient who is going for the GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test. A Genetic Counselling session will be conducted 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 GJB8.

Don’t wait any longer. Get the answers you need with the GRXCR1 Gene Deafness Autosomal Recessive Type 25 Genetic Test from DNA Labs UAE. Contact us today to schedule an appointment.

Test Name GRXCR1 Gene Deafness autosomal recessive type 25 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 GJB8
Test Details

The GRXCR1 gene is associated with deafness, specifically autosomal recessive type 25 (DFNB25). Autosomal recessive inheritance means that an individual needs to inherit two copies of the mutated gene, one from each parent, in order to develop the condition.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that analyzes multiple genes simultaneously. It uses high-throughput sequencing technology to efficiently sequence large amounts of DNA and identify genetic variations, such as mutations or changes, in the genes being analyzed.

In the context of GRXCR1 gene deafness, an NGS genetic test would involve sequencing the GRXCR1 gene to identify any variations or mutations that may be associated with autosomal recessive type 25 deafness. This test can help diagnose individuals with this specific form of deafness and provide important information for genetic counseling and management of the condition.

SKU: TEST-2712 Category:

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