EDN3 Gene Hirschsprung Disease Genetic Test
Overview
The EDN3 gene is associated with Hirschsprung disease, a congenital disorder that affects the large intestine (colon) and causes problems with bowel movements. Hirschsprung disease is characterized by the absence of nerve cells in the lower part of the colon, which leads to an obstruction and inability to pass stool.
Test Details
The EDN3 Gene Hirschsprung Disease Genetic Test is a NGS (Next-Generation Sequencing) genetic test that can be used to identify mutations or variations in the EDN3 gene that may be responsible for Hirschsprung disease. This type of testing involves sequencing the DNA of an individual to detect changes in the gene sequence that may be associated with the disease.
Components
- Test Name: EDN3 Gene Hirschsprung Disease 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: Dysmorphology
- Doctor: Pediatrics
- Test Department: Genetics
Pre Test Information
Clinical History of Patient who is going for EDN3 Gene Hirschsprung Disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EDN3 Gene Hirschsprung Disease NGS Genetic DNA Test gene EDN3.
Importance of the Test
By identifying specific mutations in the EDN3 gene, NGS genetic testing can provide a definitive diagnosis for Hirschsprung disease. This information can be used to guide treatment decisions and provide genetic counseling to affected individuals and their families. It’s important to note that Hirschsprung disease is a complex genetic disorder, and mutations in other genes may also contribute to its development. Therefore, NGS genetic testing may include analysis of multiple genes associated with the disease to provide a comprehensive evaluation.
Conclusion
The EDN3 Gene Hirschsprung Disease Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing Hirschsprung disease. With its use of NGS technology and comprehensive evaluation of multiple genes associated with the disease, this test provides accurate and reliable results. If you suspect Hirschsprung disease in yourself or a family member, consult with a pediatrician to discuss the possibility of undergoing this genetic test.
| Test Name | EDN3 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 EDN3 Gene Hirschsprung disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EDN3 Gene Hirschsprung disease NGS Genetic DNA Test gene EDN3 |
| Test Details |
The EDN3 gene is associated with Hirschsprung disease, a congenital disorder that affects the large intestine (colon) and causes problems with bowel movements. Hirschsprung disease is characterized by the absence of nerve cells in the lower part of the colon, which leads to an obstruction and inability to pass stool. NGS (Next-Generation Sequencing) genetic testing can be used to identify mutations or variations in the EDN3 gene that may be responsible for Hirschsprung disease. This type of testing involves sequencing the DNA of an individual to detect changes in the gene sequence that may be associated with the disease. By identifying specific mutations in the EDN3 gene, NGS genetic testing can provide a definitive diagnosis for Hirschsprung disease. This information can be used to guide treatment decisions and provide genetic counseling to affected individuals and their families. It’s important to note that Hirschsprung disease is a complex genetic disorder, and mutations in other genes may also contribute to its development. Therefore, NGS genetic testing may include analysis of multiple genes associated with the disease to provide a comprehensive evaluation. |
