MKS1 Gene Bardet-Biedl Syndrome Type 13 Genetic Test
At DNA Labs UAE, we offer the MKS1 Gene Bardet-Biedl Syndrome Type 13 Genetic Test at a price of 4400.0 AED. This test is used to diagnose Bardet-Biedl syndrome type 13, a rare genetic disorder characterized by symptoms such as obesity, vision loss, kidney abnormalities, intellectual disability, and polydactyly (extra fingers or toes).
Test Components and Details
- Test Name: MKS1 Gene Bardet-Biedl Syndrome Type 13 Genetic Test
- 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 MKS1 Gene Bardet-Biedl Syndrome Type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MKS1 Gene Bardet-Biedl Syndrome Type 13 NGS Genetic DNA Test gene MKS1
About the MKS1 Gene and NGS Genetic Testing
The MKS1 gene is associated with Bardet-Biedl Syndrome Type 13. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic mutations or variants. In the case of Bardet-Biedl Syndrome Type 13, NGS genetic testing can be used to analyze the MKS1 gene for any mutations or variants that may be present.
By identifying specific genetic mutations or variants in the MKS1 gene, NGS genetic testing can help confirm a diagnosis of Bardet-Biedl Syndrome Type 13 and provide information about the specific genetic cause of the disorder. This information can be useful for genetic counseling, family planning, and potentially for the development of targeted treatments in the future.
| Test Name | MKS1 Gene Bardet-Biedl syndrome type 13 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 MKS1 Gene Bardet-Biedl syndrome type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MKS1 Gene Bardet-Biedl syndrome type 13 NGS Genetic DNA Test gene MKS1 |
| Test Details | The MKS1 gene is associated with Bardet-Biedl syndrome type 13. Bardet-Biedl syndrome is a rare genetic disorder characterized by a combination of symptoms including obesity, vision loss, kidney abnormalities, intellectual disability, and polydactyly (extra fingers or toes). NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic mutations or variants. In the case of Bardet-Biedl syndrome type 13, NGS genetic testing can be used to analyze the MKS1 gene for any mutations or variants that may be present. By identifying specific genetic mutations or variants in the MKS1 gene, NGS genetic testing can help confirm a diagnosis of Bardet-Biedl syndrome type 13 and provide information about the specific genetic cause of the disorder. This can be useful for genetic counseling, family planning, and potentially for the development of targeted treatments in the future. |
