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RET Gene Hirschsprung Disease Genetic Test

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

-21%

The RET Gene Hirschsprung Disease Genetic Test is a specialized diagnostic examination conducted to identify mutations in the RET gene, which are strongly associated with Hirschsprung Disease (HSCR). Hirschsprung Disease is a congenital disorder characterized by the absence of nerve cells in parts of the intestine, leading to severe constipation or intestinal obstruction. The RET gene plays a crucial role in the development of the enteric nervous system, and mutations in this gene can lead to the symptoms associated with HSCR.

This genetic test is particularly important for individuals showing symptoms of Hirschsprung Disease or for those who have a family history of the condition, as it can confirm the diagnosis and help in the planning of appropriate treatment strategies. It involves the collection of a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific mutations in the RET gene.

Conducted at DNA Labs UAE, a leading facility in genetic testing, the test ensures accuracy and reliability in the detection of RET gene mutations. The cost of the RET Gene Hirschsprung Disease Genetic Test is set at 4400 AED. This investment can provide critical information for affected individuals and their families, offering insights into the genetic underpinnings of the condition and guiding decisions regarding management and care.

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RET Gene Hirschsprung disease Genetic Test

Components: RET 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 RET Gene Hirschsprung disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RET Gene Hirschsprung disease NGS Genetic DNA Test gene RET

Test Details

The RET 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 certain parts of the colon, leading to a blockage of stool and a variety of symptoms, including constipation, abdominal distension, and failure to thrive.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual’s genes. In the context of Hirschsprung disease, NGS genetic testing can be used to identify mutations or variations in the RET gene that may be associated with the condition.

NGS genetic testing for Hirschsprung disease can be performed using various methods, such as targeted gene panel sequencing or whole-exome sequencing. These tests can identify specific genetic changes in the RET gene that are known to be associated with Hirschsprung disease.

By analyzing the DNA sequence of the RET gene, NGS testing can help diagnose individuals with Hirschsprung disease and provide valuable information for genetic counseling and treatment decisions.

It is important to note that NGS genetic testing for Hirschsprung disease is typically performed in specialized laboratories and requires a physician’s order. The results of the test should be interpreted by a healthcare professional with expertise in genetics to provide accurate diagnosis and appropriate management recommendations.

Test Name RET 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 RET Gene Hirschsprung disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RET Gene Hirschsprung disease NGS Genetic DNA Test gene RET
Test Details

The RET 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 certain parts of the colon, leading to a blockage of stool and a variety of symptoms, including constipation, abdominal distension, and failure to thrive.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual’s genes. In the context of Hirschsprung disease, NGS genetic testing can be used to identify mutations or variations in the RET gene that may be associated with the condition.

NGS genetic testing for Hirschsprung disease can be performed using various methods, such as targeted gene panel sequencing or whole-exome sequencing. These tests can identify specific genetic changes in the RET gene that are known to be associated with Hirschsprung disease. By analyzing the DNA sequence of the RET gene, NGS testing can help diagnose individuals with Hirschsprung disease and provide valuable information for genetic counseling and treatment decisions.

It is important to note that NGS genetic testing for Hirschsprung disease is typically performed in specialized laboratories and requires a physician’s order. The results of the test should be interpreted by a healthcare professional with expertise in genetics to provide accurate diagnosis and appropriate management recommendations.