NEUROG3 Gene Diarrhea Type 4 Malabsorptive Congenital Genetic Test
Test Name: NEUROG3 Gene Diarrhea Type 4 Malabsorptive Congenital 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: Metabolic Disorders
Doctor: General Physician
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for NEUROG3 Gene Diarrhea Type 4, Malabsorptive, Congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Diarrhea Type 4, Malabsorptive, Congenital.
Test Details
The NEUROG3 gene is responsible for encoding a protein called Neurogenin 3, which plays a crucial role in the development of the endocrine cells in the pancreas and the intestine. Mutations in the NEUROG3 gene can lead to various disorders, including a type of diarrhea known as malabsorptive diarrhea type 4.
Malabsorptive diarrhea refers to a condition where the intestines are unable to properly absorb nutrients from food, leading to chronic diarrhea and malnutrition. Malabsorptive diarrhea type 4 specifically refers to a congenital form of the condition, meaning it is present from birth.
NGS genetic testing, also known as Next-Generation Sequencing, is a type of genetic test that can analyze multiple genes simultaneously to identify mutations or variations that may be associated with a particular disorder. In the case of malabsorptive diarrhea type 4, NGS genetic testing can be used to identify mutations in the NEUROG3 gene that may be causing the condition.
By identifying the specific genetic mutation causing malabsorptive diarrhea type 4, NGS genetic testing can help with diagnosis, prognosis, and potentially guide treatment options. It can also provide valuable information for genetic counseling and family planning.
It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support based on the test results.
| Test Name | NEUROG3 Gene Diarrhea type 4 malabsorptive congenital 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for NEUROG3 Gene Diarrhea type 4, malabsorptive, congenital NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Diarrhea type 4, malabsorptive, congenital |
| Test Details |
The NEUROG3 gene is responsible for encoding a protein called Neurogenin 3, which plays a crucial role in the development of the endocrine cells in the pancreas and the intestine. Mutations in the NEUROG3 gene can lead to various disorders, including a type of diarrhea known as malabsorptive diarrhea type 4. Malabsorptive diarrhea refers to a condition where the intestines are unable to properly absorb nutrients from food, leading to chronic diarrhea and malnutrition. Malabsorptive diarrhea type 4 specifically refers to a congenital form of the condition, meaning it is present from birth. NGS genetic testing, also known as Next-Generation Sequencing, is a type of genetic test that can analyze multiple genes simultaneously to identify mutations or variations that may be associated with a particular disorder. In the case of malabsorptive diarrhea type 4, NGS genetic testing can be used to identify mutations in the NEUROG3 gene that may be causing the condition. By identifying the specific genetic mutation causing malabsorptive diarrhea type 4, NGS genetic testing can help with diagnosis, prognosis, and potentially guide treatment options. It can also provide valuable information for genetic counseling and family planning. It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support based on the test results. |
