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. |