BBS2 Gene Bardet-Biedl syndrome type 2 Genetic Test
Test Name: BBS2 Gene Bardet-Biedl syndrome type 2 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 BBS2 Gene Bardet-Biedl syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS2 Gene Bardet-Biedl syndrome type 2 NGS Genetic DNA Test gene BBS2
Test Details
The BBS2 gene is associated with Bardet-Biedl syndrome type 2 (BBS2), a rare genetic disorder characterized by various symptoms including obesity, vision problems, kidney abnormalities, intellectual disability, and extra fingers or toes.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of BBS2, NGS genetic testing can identify any mutations or changes in the BBS2 gene that may be responsible for causing Bardet-Biedl syndrome type 2. This type of testing can help in diagnosing individuals with BBS2 and provide valuable information for genetic counseling and family planning.
The NGS genetic test for BBS2 involves collecting a sample of DNA, typically through a blood or saliva sample, and analyzing it using advanced sequencing technology. The DNA is sequenced to identify any variations or mutations in the BBS2 gene. The results of the test can help confirm a diagnosis of BBS2 and guide appropriate medical management and treatment options.
It is important to note that genetic testing for BBS2 should be performed by a qualified healthcare professional or genetic counselor who can interpret the results accurately and provide appropriate counseling and support.
| Test Name | BBS2 Gene Bardet-Biedl syndrome type 2 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 BBS2 Gene Bardet-Biedl syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS2 Gene Bardet-Biedl syndrome type 2 NGS Genetic DNA Test gene BBS2 |
| Test Details |
The BBS2 gene is associated with Bardet-Biedl syndrome type 2 (BBS2), a rare genetic disorder characterized by various symptoms including obesity, vision problems, kidney abnormalities, intellectual disability, and extra fingers or toes. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of BBS2, NGS genetic testing can identify any mutations or changes in the BBS2 gene that may be responsible for causing Bardet-Biedl syndrome type 2. This type of testing can help in diagnosing individuals with BBS2 and provide valuable information for genetic counseling and family planning. The NGS genetic test for BBS2 involves collecting a sample of DNA, typically through a blood or saliva sample, and analyzing it using advanced sequencing technology. The DNA is sequenced to identify any variations or mutations in the BBS2 gene. The results of the test can help confirm a diagnosis of BBS2 and guide appropriate medical management and treatment options. It is important to note that genetic testing for BBS2 should be performed by a qualified healthcare professional or genetic counselor who can interpret the results accurately and provide appropriate counseling and support. |
