BBS10 Gene Bardet-Biedl Syndrome Type 10 Genetic Test
Test Name: BBS10 Gene Bardet-Biedl Syndrome Type 10 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 BBS10 Gene Bardet-Biedl Syndrome Type 10 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS10 Gene Bardet-Biedl Syndrome Type 10 NGS Genetic DNA Test gene BBS10
Test Details: The BBS10 gene is associated with Bardet-Biedl Syndrome Type 10, a rare genetic disorder that affects multiple organ systems. Bardet-Biedl Syndrome is characterized by a range of symptoms including obesity, vision problems, kidney abnormalities, extra fingers or toes, and intellectual disability. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the identification of specific genetic variants or mutations that may be present in an individual’s DNA. In the case of BBS10, NGS genetic testing can be used to detect any mutations or variants in the BBS10 gene that may be causing Bardet-Biedl Syndrome Type 10. This type of genetic testing can be helpful in confirming a diagnosis, providing information about disease progression and potential complications, and guiding treatment and management options. It may also be used for carrier testing in individuals with a family history of Bardet-Biedl Syndrome or for prenatal testing in families at risk of having a child with the condition. It is important to note that genetic testing should always be done in consultation with a healthcare professional or genetic counselor, who can provide guidance and support throughout the testing process and help interpret the results.
| Test Name | BBS10 Gene Bardet-Biedl syndrome type 10 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 BBS10 Gene Bardet-Biedl syndrome type 10 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS10 Gene Bardet-Biedl syndrome type 10 NGS Genetic DNA Test gene BBS10 |
| Test Details | The BBS10 gene is associated with Bardet-Biedl syndrome type 10, a rare genetic disorder that affects multiple organ systems. Bardet-Biedl syndrome is characterized by a range of symptoms including obesity, vision problems, kidney abnormalities, extra fingers or toes, and intellectual disability. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the identification of specific genetic variants or mutations that may be present in an individual’s DNA. In the case of BBS10, NGS genetic testing can be used to detect any mutations or variants in the BBS10 gene that may be causing Bardet-Biedl syndrome type 10. This type of genetic testing can be helpful in confirming a diagnosis, providing information about disease progression and potential complications, and guiding treatment and management options. It may also be used for carrier testing in individuals with a family history of Bardet-Biedl syndrome or for prenatal testing in families at risk of having a child with the condition. It is important to note that genetic testing should always be done in consultation with a healthcare professional or genetic counselor, who can provide guidance and support throughout the testing process and help interpret the results. |
