SLC10A2 Gene Bile Acid Malabsorption Primary NGS Genetic DNA Test
Introduction
The SLC10A2 Gene Bile Acid Malabsorption Primary NGS Genetic DNA Test is a crucial diagnostic tool for identifying genetic conditions related to bile acid absorption. This test utilizes Next Generation Sequencing (NGS) technology to analyze the SLC10A2 gene, which plays a vital role in the absorption of bile acids in the intestine. Understanding the genetic factors that contribute to bile acid malabsorption can significantly impact treatment decisions and improve patient outcomes.
What the Test Measures
This genetic test specifically measures mutations in the SLC10A2 gene. By detecting variations in this gene, healthcare providers can determine the likelihood of bile acid malabsorption, a condition that can lead to gastrointestinal symptoms and metabolic disorders.
Who Should Consider This Test
Individuals experiencing symptoms such as chronic diarrhea, abdominal pain, or unexplained weight loss may benefit from this test. Additionally, those with a family history of metabolic disorders or bile acid malabsorption should consider undergoing genetic testing to assess their risk.
Benefits of Taking the Test
- Early identification of genetic predispositions to bile acid malabsorption.
- Informed decision-making regarding dietary and medical management.
- Personalized treatment plans based on genetic insights.
- Improved quality of life by addressing underlying health issues.
Understanding Your Results
Results from the SLC10A2 Gene Bile Acid Malabsorption Primary NGS Genetic DNA Test will indicate whether genetic mutations are present. A genetic counseling session is recommended to help interpret the results and discuss potential implications for you and your family.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SLC10A2 Gene Bile Acid Malabsorption Primary NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Booking the Test
To book your SLC10A2 Gene Bile Acid Malabsorption Primary NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you in scheduling your appointment and answering any questions you may have.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected with bile acid malabsorption.
Specialty and Department
This test falls under the specialty of General Physician and the department of Genetics, utilizing NGS technology to diagnose metabolic disorders.
