ECE1 Gene Hirschsprung disease Genetic Test
At DNA Labs UAE, we offer the ECE1 Gene Hirschsprung disease Genetic Test at a cost of 4400.0 AED. This test is used to diagnose Hirschsprung disease, a congenital condition that affects the large intestine and causes problems with bowel movements.
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
Before undergoing the ECE1 Gene Hirschsprung disease NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by Hirschsprung disease and the ECE1 gene.
Test Details
The ECE1 gene is associated with Hirschsprung disease, a condition that affects the colon and causes difficulties with bowel movements. NGS (Next-Generation Sequencing) is a genetic testing technique that allows for the analysis of multiple genes simultaneously.
In the context of Hirschsprung disease, NGS genetic testing can identify mutations or variations in the ECE1 gene that may be linked to the condition. By analyzing the DNA sequence of the ECE1 gene, NGS testing provides information about any genetic changes that may be present, aiding in the diagnosis and understanding of Hirschsprung disease.
NGS genetic testing for Hirschsprung disease can be performed on individuals with symptoms consistent with the condition and their family members who may be at risk of carrying the genetic mutation. It can also be used for prenatal testing to determine if a fetus is at risk of developing Hirschsprung disease.
Overall, NGS genetic testing of the ECE1 gene is a valuable tool in diagnosing and understanding Hirschsprung disease, allowing for more accurate and personalized treatment and management of the condition.
| Test Name | ECE1 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 ECE1 Gene Hirschsprung disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ECE1 Gene Hirschsprung disease NGS Genetic DNA Test gene ECE1 |
| Test Details |
The ECE1 gene is a gene that is associated with Hirschsprung disease. Hirschsprung disease is a congenital condition that affects the large intestine (colon) and causes problems with bowel movements. It occurs when certain nerve cells in the colon are missing, which leads to a blockage of stool and difficulty passing it. NGS (Next-Generation Sequencing) is a genetic testing technique that allows for the analysis of multiple genes simultaneously. In the context of Hirschsprung disease, NGS genetic testing can be used to identify mutations or variations in the ECE1 gene that may be associated with the condition. By analyzing the DNA sequence of the ECE1 gene, NGS testing can provide information about any genetic changes that may be present. This can help in diagnosing Hirschsprung disease and determining the underlying cause of the condition. NGS genetic testing for Hirschsprung disease can be performed on individuals who have symptoms consistent with the condition, as well as on their family members who may be at risk of carrying the genetic mutation. It can also be used for prenatal testing to determine if a fetus is at risk of developing Hirschsprung disease. Overall, NGS genetic testing of the ECE1 gene is a valuable tool in diagnosing and understanding Hirschsprung disease, allowing for more accurate and personalized treatment and management of the condition. |
