AKR1D1 Gene Bile Acid Synthesis Defect Type 2 Congenital NGS Genetic DNA Test
The AKR1D1 Gene Bile Acid Synthesis Defect Type 2 Congenital NGS Genetic DNA Test is a vital diagnostic tool that helps identify genetic mutations associated with metabolic disorders, particularly those affecting bile acid synthesis. This test utilizes Next Generation Sequencing (NGS) technology to provide accurate and comprehensive results, enabling healthcare professionals to make informed decisions regarding patient care.
What the Test Measures
This genetic test specifically measures mutations in the AKR1D1 gene, which are responsible for congenital bile acid synthesis defects. By analyzing the genetic material, the test can detect any abnormalities that may lead to metabolic disorders.
Who Should Consider This Test
- Individuals with a family history of bile acid synthesis defects.
- Patients exhibiting symptoms of metabolic disorders, such as jaundice, liver dysfunction, or unexplained gastrointestinal issues.
- Those undergoing genetic counseling for hereditary conditions.
Benefits of Taking the Test
- Early detection and diagnosis of metabolic disorders.
- Informed treatment options based on genetic findings.
- Guidance for family planning and management of hereditary conditions.
Understanding Your Results
Results from the AKR1D1 Gene Bile Acid Synthesis Defect Type 2 test will be provided in a clear and concise format. It is important to discuss these results with your healthcare provider, who can explain their implications and guide you on the next steps.
Test Name and Price
| Discount Price | Regular Price |
|---|---|
| 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to understand your genetic health. Book the AKR1D1 Gene Bile Acid Synthesis Defect Type 2 Congenital NGS Genetic DNA Test today by calling or WhatsApp at +2348077798758. Our team at DNA Labs Nigeria is here to assist you with any questions and guide you through the testing process.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood
Pre-Test Instructions: Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with bile acid synthesis defect type 2.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Metabolic Disorders
