RAB3GAP2 Gene Martsolf syndrome 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: Dysmorphology
- Doctor: Pediatrics
- Test Department: Genetics
Pre Test Information
Clinical History of Patient who is going for RAB3GAP2 Gene Martsolf syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAB3GAP2 Gene Martsolf syndrome NGS Genetic DNA Test gene RAB3GAP2.
Test Details
The RAB3GAP2 gene is associated with Martsolf syndrome, which is a rare genetic disorder characterized by intellectual disability, developmental delay, hearing loss, and other physical abnormalities.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously, providing a comprehensive analysis of an individual’s genetic makeup. In the case of Martsolf syndrome, NGS genetic testing can be used to identify mutations or variations in the RAB3GAP2 gene that may be causing the disorder. This can help with diagnosis, genetic counseling, and potentially guiding treatment options for affected individuals and their families.
Test Name | RAB3GAP2 Gene Martsolf syndrome 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 | Dysmorphology |
Doctor | Pediatrics |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for RAB3GAP2 Gene Martsolf syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAB3GAP2 Gene Martsolf syndrome NGS Genetic DNA Test gene RAB3GAP2 |
Test Details |
The RAB3GAP2 gene is associated with Martsolf syndrome, which is a rare genetic disorder characterized by intellectual disability, developmental delay, hearing loss, and other physical abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously, providing a comprehensive analysis of an individual’s genetic makeup. In the case of Martsolf syndrome, NGS genetic testing can be used to identify mutations or variations in the RAB3GAP2 gene that may be causing the disorder. This can help with diagnosis, genetic counseling, and potentially guiding treatment options for affected individuals and their families. |