SLC10A2 Gene Bile Acid Malabsorption Primary Genetic Test
Cost: 4400.0 AED
Symptoms, Diagnosis, and Test Details
The SLC10A2 gene is responsible for encoding a protein called the sodium/bile acid cotransporter (ASBT), which plays a crucial role in the absorption of bile acids in the small intestine. Bile acids are produced by the liver and are essential for the digestion and absorption of dietary fats.
Bile acid malabsorption (BAM) is a condition characterized by impaired absorption of bile acids in the small intestine, leading to an increase in the amount of bile acids in the colon. This can result in symptoms such as chronic diarrhea, abdominal pain, bloating, and malnutrition.
Primary NGS (Next-Generation Sequencing) genetic testing refers to the use of advanced DNA sequencing technologies to analyze multiple genes simultaneously. In the context of bile acid malabsorption, primary NGS genetic testing can be used to identify mutations or variants in the SLC10A2 gene that may be responsible for the condition.
By identifying specific genetic changes in the SLC10A2 gene, primary NGS genetic testing can help diagnose individuals with bile acid malabsorption and provide valuable information for personalized treatment and management strategies. It can also aid in genetic counseling and family planning for individuals with a family history of the condition.
Overall, primary NGS genetic testing for the SLC10A2 gene can contribute to a better understanding of the underlying genetic causes of bile acid malabsorption and improve patient care and outcomes.
Test Information
- Test Name: SLC10A2 Gene Bile Acid Malabsorption Primary Genetic Test
- Components: NGS Technology
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Test Type: Metabolic Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information
A Genetic Counselling session is required to draw a pedigree chart of family members affected with Bile Acid Malabsorption, primary before undergoing the SLC10A2 Gene Bile Acid Malabsorption Primary Genetic Test.
| Test Name | SLC10A2 Gene Bile acid malabsorption primary 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 SLC10A2 Gene Bile acid malabsorption, primary NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Bile acid malabsorption, primary |
| Test Details |
The SLC10A2 gene is responsible for encoding a protein called the sodium/bile acid cotransporter (ASBT), which plays a crucial role in the absorption of bile acids in the small intestine. Bile acids are produced by the liver and are essential for the digestion and absorption of dietary fats. Bile acid malabsorption (BAM) is a condition characterized by impaired absorption of bile acids in the small intestine, leading to an increase in the amount of bile acids in the colon. This can result in symptoms such as chronic diarrhea, abdominal pain, bloating, and malnutrition. Primary NGS (Next-Generation Sequencing) genetic testing refers to the use of advanced DNA sequencing technologies to analyze multiple genes simultaneously. In the context of bile acid malabsorption, primary NGS genetic testing can be used to identify mutations or variants in the SLC10A2 gene that may be responsible for the condition. By identifying specific genetic changes in the SLC10A2 gene, primary NGS genetic testing can help diagnose individuals with bile acid malabsorption and provide valuable information for personalized treatment and management strategies. It can also aid in genetic counseling and family planning for individuals with a family history of the condition. Overall, primary NGS genetic testing for the SLC10A2 gene can contribute to a better understanding of the underlying genetic causes of bile acid malabsorption and improve patient care and outcomes. |
