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ECE1 Gene Hirschsprung Disease Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The ECE1 Gene Hirschsprung Disease Genetic Test is a specialized diagnostic tool used to detect mutations in the ECE1 gene, which are associated with Hirschsprung Disease (HD). Hirschsprung Disease is a congenital condition characterized by the absence of nerve cells (ganglia) in a portion of the intestine, leading to severe constipation or intestinal obstruction. The ECE1 gene plays a crucial role in the development of the enteric nervous system, and mutations in this gene can lead to the development of HD.

This genetic test involves analyzing the patient’s DNA to identify any mutations in the ECE1 gene that might be responsible for the condition. Early detection through genetic testing can provide valuable information for managing the disease, guiding treatment options, and offering insight into the risk of the condition being passed on to future generations.

The ECE1 Gene Hirschsprung Disease Genetic Test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the expertise required to accurately interpret the results. By opting for this test at DNA Labs UAE, patients and their families can expect comprehensive support, from sample collection to result interpretation, aiding in the effective management of Hirschsprung Disease.

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  • This test is not intended for medical diagnosis or treatment
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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.

SKU: TEST-4145 Category:

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