NRG1 Gene Hirschsprung disease Genetic Test
Test Name: NRG1 Gene Hirschsprung disease 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: Dysmorphology
Doctor: Pediatrics
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for NRG1 Gene Hirschsprung disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NRG1 Gene Hirschsprung disease NGS Genetic DNA Test gene NRG1
Test Details
The NRG1 gene is not directly associated with Hirschsprung disease. Hirschsprung disease is a congenital disorder characterized by the absence of nerve cells in the muscles of the colon, leading to difficulties in passing stool. It is primarily caused by mutations in the RET gene.
NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and identify genetic variations that may be associated with a particular condition. In the context of Hirschsprung disease, NGS can be used to identify mutations in the RET gene and other genes known to be involved in the development of this disorder. By analyzing a panel of genes associated with Hirschsprung disease, NGS can provide a comprehensive assessment of genetic variations that may contribute to the condition. This information can be useful for diagnosis, risk assessment, and genetic counseling.
| Test Name | NRG1 Gene Hirschsprung disease 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 NRG1 Gene Hirschsprung disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NRG1 Gene Hirschsprung disease NGS Genetic DNA Test gene NRG1 |
| Test Details |
The NRG1 gene is not directly associated with Hirschsprung disease. Hirschsprung disease is a congenital disorder characterized by the absence of nerve cells in the muscles of the colon, leading to difficulties in passing stool. It is primarily caused by mutations in the RET gene. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and identify genetic variations that may be associated with a particular condition. In the context of Hirschsprung disease, NGS can be used to identify mutations in the RET gene and other genes known to be involved in the development of this disorder. By analyzing a panel of genes associated with Hirschsprung disease, NGS can provide a comprehensive assessment of genetic variations that may contribute to the condition. This information can be useful for diagnosis, risk assessment, and genetic counseling. |
