TTC8 Gene Bardet-Biedl Syndrome Type 8 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: Hepatology Nephrology Endocrinology Disorders
Doctor: General Physician
Test Department: Genetics
Pre Test Information
Clinical History of Patient who is going for TTC8 Gene Bardet-Biedl Syndrome Type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TTC8 Gene Bardet-Biedl Syndrome Type 8 NGS Genetic DNA Test gene TTC8.
Test Details
The TTC8 gene is associated with Bardet-Biedl Syndrome Type 8 (BBS8). Bardet-Biedl Syndrome is a rare genetic disorder characterized by a combination of symptoms including obesity, vision problems, kidney abnormalities, intellectual disability, and other physical and developmental abnormalities.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of an individual’s genetic makeup. In the context of Bardet-Biedl Syndrome, NGS genetic testing can be used to identify mutations in the TTC8 gene, which is one of the genes known to be associated with the condition.
By analyzing the DNA sequence of the TTC8 gene, NGS genetic testing can help diagnose Bardet-Biedl Syndrome Type 8 and provide valuable information about the specific genetic changes present in an individual. This information can be used for genetic counseling, family planning, and potentially targeted treatments or interventions.
Test Name | TTC8 Gene Bardet-Biedl syndrome type 8 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 | Hepatology Nephrology Endocrinology Disorders |
Doctor | General Physician |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for TTC8 Gene Bardet-Biedl syndrome type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TTC8 Gene Bardet-Biedl syndrome type 8 NGS Genetic DNA Test gene TTC8 |
Test Details |
The TTC8 gene is associated with Bardet-Biedl syndrome type 8 (BBS8). Bardet-Biedl syndrome is a rare genetic disorder characterized by a combination of symptoms including obesity, vision problems, kidney abnormalities, intellectual disability, and other physical and developmental abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of an individual’s genetic makeup. In the context of Bardet-Biedl syndrome, NGS genetic testing can be used to identify mutations in the TTC8 gene, which is one of the genes known to be associated with the condition. By analyzing the DNA sequence of the TTC8 gene, NGS genetic testing can help diagnose Bardet-Biedl syndrome type 8 and provide valuable information about the specific genetic changes present in an individual. This information can be used for genetic counseling, family planning, and potentially targeted treatments or interventions. |