PJVK Gene Deafness Autosomal Recessive Type 59 Genetic Test
Cost: AED 4400.0
Components:
- Price: AED 4400.0
- 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 GJB10.
Test Details:
The PJVK gene is associated with deafness, specifically autosomal recessive type 59 (DFNB59). This type of deafness is inherited in an autosomal recessive manner, meaning 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 type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of PJVK gene deafness, NGS genetic testing can be used to identify mutations or variations in the PJVK gene that may be responsible for causing DFNB59.
By analyzing the PJVK gene using NGS technology, healthcare professionals can determine if an individual carries mutations in this gene and, therefore, has an increased risk of developing DFNB59. This information can be useful for genetic counseling, family planning, and potentially for developing targeted therapies in the future.
It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate interpretation and counseling based on the results.
| Test Name | PJVK Gene Deafness autosomal recessive type 59 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 GJB10 |
| Test Details |
The PJVK gene is associated with deafness, specifically autosomal recessive type 59 (DFNB59). This type of deafness is inherited in an autosomal recessive manner, meaning 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 type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of PJVK gene deafness, NGS genetic testing can be used to identify mutations or variations in the PJVK gene that may be responsible for causing DFNB59. By analyzing the PJVK gene using NGS technology, healthcare professionals can determine if an individual carries mutations in this gene and, therefore, has an increased risk of developing DFNB59. This information can be useful for genetic counseling, family planning, and potentially for developing targeted therapies in the future. It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate interpretation and counseling based on the results. |
