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KIF1BP Gene Hirschsprung Disease Genetic Test Cost

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

-21%

The KIF1BP gene Hirschsprung disease genetic test is a specialized diagnostic tool designed to identify mutations in the KIF1BP gene, which have been associated with Hirschsprung disease. Hirschsprung disease is a congenital condition characterized by the absence of nerve cells (ganglia) in a segment of the bowel, leading to severe constipation, intestinal obstruction, and difficulty with bowel movements. This genetic test is crucial for early diagnosis and management of the condition, potentially guiding surgical and medical treatment options.

Performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test offers a comprehensive analysis of the KIF1BP gene to detect any genetic abnormalities that could indicate a predisposition to Hirschsprung disease. The cost of the test is 4400 AED, reflecting the intricate technology and expertise required to conduct this sophisticated analysis. By opting for this test, patients and their families can gain valuable insights into their genetic makeup, enabling informed decisions about their health and medical care.

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  • This test is not intended for medical diagnosis or treatment
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KIF1BP Gene Hirschsprung Disease Genetic Test

Test Name: KIF1BP 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 KIF1BP Gene Hirschsprung Disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KIF1BP Gene Hirschsprung Disease NGS Genetic DNA Test gene KIF1BP

Test Details

The KIF1BP gene is not directly associated with Hirschsprung disease. Hirschsprung disease is a congenital disorder characterized by the absence of nerve cells in parts of the intestine, leading to difficulties in passing stool. It is primarily caused by mutations in the RET gene.

NGS (Next-Generation Sequencing) genetic tests are a type of genetic testing that can analyze multiple genes simultaneously. These tests can be used to identify mutations or variations in genes that may be associated with a particular condition or disease. In the case of Hirschsprung disease, NGS genetic testing can be used to identify mutations in the RET gene, as well as other genes that may be less commonly associated with the condition.

However, it is important to note that genetic testing for Hirschsprung disease is typically not the first step in diagnosis. Diagnosis is usually based on clinical symptoms and physical examination. Genetic testing may be used to confirm a suspected diagnosis or in cases where there is a family history of the condition.

Genetic counseling is often recommended before and after genetic testing to help individuals understand the implications of the results.

Test Name KIF1BP 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 KIF1BP Gene Hirschsprung disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KIF1BP Gene Hirschsprung disease NGS Genetic DNA Test gene KIF1BP
Test Details

The KIF1BP gene is not directly associated with Hirschsprung disease. Hirschsprung disease is a congenital disorder characterized by the absence of nerve cells in parts of the intestine, leading to difficulties in passing stool. It is primarily caused by mutations in the RET gene.

NGS (Next-Generation Sequencing) genetic tests are a type of genetic testing that can analyze multiple genes simultaneously. These tests can be used to identify mutations or variations in genes that may be associated with a particular condition or disease. In the case of Hirschsprung disease, NGS genetic testing can be used to identify mutations in the RET gene, as well as other genes that may be less commonly associated with the condition.

However, it is important to note that genetic testing for Hirschsprung disease is typically not the first step in diagnosis. Diagnosis is usually based on clinical symptoms and physical examination. Genetic testing may be used to confirm a suspected diagnosis or in cases where there is a family history of the condition. Genetic counseling is often recommended before and after genetic testing to help individuals understand the implications of the results.