BBS12 Gene Bardet-Biedl Syndrome Type 12 Genetic Test
Cost: AED 4400.0
Test 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: Hepatology Nephrology Endocrinology Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information:
Clinical History of Patient who is going for BBS12 Gene Bardet-Biedl Syndrome Type 12 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS12 Gene Bardet-Biedl Syndrome Type 12 NGS Genetic DNA Test gene BBS12.
Test Details:
The BBS12 gene is associated with Bardet-Biedl Syndrome Type 12, a rare genetic disorder characterized by a variety of symptoms including obesity, vision problems, kidney abnormalities, intellectual disability, and polydactyly (extra fingers or toes). NGS (Next-Generation Sequencing) genetic testing is a method used to analyze and sequence a person’s DNA to identify any genetic variations or mutations that may be present in the BBS12 gene.
This test can help confirm a diagnosis of Bardet-Biedl Syndrome Type 12 and provide information about the specific genetic changes that may be causing the condition. It can also be used for carrier testing and prenatal diagnosis in families with a known BBS12 gene mutation.
Test Name | BBS12 Gene Bardet-Biedl syndrome type 12 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 BBS12 Gene Bardet-Biedl syndrome type 12 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS12 Gene Bardet-Biedl syndrome type 12 NGS Genetic DNA Test gene BBS12 |
Test Details |
The BBS12 gene is associated with Bardet-Biedl syndrome type 12, a rare genetic disorder characterized by a variety of symptoms including obesity, vision problems, kidney abnormalities, intellectual disability, and polydactyly (extra fingers or toes). NGS (Next-Generation Sequencing) genetic testing is a method used to analyze and sequence a person’s DNA to identify any genetic variations or mutations that may be present in the BBS12 gene. This test can help confirm a diagnosis of Bardet-Biedl syndrome type 12 and provide information about the specific genetic changes that may be causing the condition. It can also be used for carrier testing and prenatal diagnosis in families with a known BBS12 gene mutation. |