TRIM32 Gene Bardet-Biedl Syndrome Type 11 Genetic Test
Test Name: TRIM32 Gene Bardet-Biedl syndrome type 11 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
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 TRIM32 Gene Bardet-Biedl syndrome type 11 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TRIM32 Gene Bardet-Biedl syndrome type 11 NGS Genetic DNA Test gene TRIM32
Test Details
The TRIM32 gene is associated with Bardet-Biedl syndrome type 11 (BBS11). Bardet-Biedl syndrome is a rare genetic disorder characterized by a variety of symptoms, including obesity, vision problems, kidney abnormalities, and intellectual disability. BBS11 is caused by mutations in the TRIM32 gene.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes. It is a highly efficient and accurate method for identifying genetic variations and mutations associated with various genetic disorders, including Bardet-Biedl syndrome.
A TRIM32 gene Bardet-Biedl syndrome type 11 NGS genetic test involves sequencing the TRIM32 gene to identify any mutations or variations that may be responsible for causing BBS11. This test can help in confirming a diagnosis of BBS11 in individuals who exhibit symptoms of the disorder.
Genetic testing for BBS11 can provide important information for patients and their families, including a definitive diagnosis, prognosis, and potential treatment options. It can also help in genetic counseling and family planning decisions. However, it is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals.
| Test Name | TRIM32 Gene Bardet-Biedl syndrome type 11 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 TRIM32 Gene Bardet-Biedl syndrome type 11 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TRIM32 Gene Bardet-Biedl syndrome type 11 NGS Genetic DNA Test gene TRIM32 |
| Test Details |
The TRIM32 gene is associated with Bardet-Biedl syndrome type 11 (BBS11). Bardet-Biedl syndrome is a rare genetic disorder characterized by a variety of symptoms, including obesity, vision problems, kidney abnormalities, and intellectual disability. BBS11 is caused by mutations in the TRIM32 gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes. It is a highly efficient and accurate method for identifying genetic variations and mutations associated with various genetic disorders, including Bardet-Biedl syndrome. A TRIM32 gene Bardet-Biedl syndrome type 11 NGS genetic test involves sequencing the TRIM32 gene to identify any mutations or variations that may be responsible for causing BBS11. This test can help in confirming a diagnosis of BBS11 in individuals who exhibit symptoms of the disorder. Genetic testing for BBS11 can provide important information for patients and their families, including a definitive diagnosis, prognosis, and potential treatment options. It can also help in genetic counseling and family planning decisions. However, it is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals. |
