BAAT Gene Hypercholanemia NGS Genetic DNA Test
Introduction
The BAAT Gene Hypercholanemia NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to analyze genetic variations associated with hypercholanemia, a metabolic disorder. This test is crucial for individuals with a family history of metabolic conditions and provides valuable insights into one’s genetic predisposition.
What the Test Measures
This test specifically measures genetic mutations in the BAAT gene, which are linked to the metabolism of bile acids. By identifying these mutations, healthcare providers can better understand the risk of hypercholanemia and related metabolic disorders.
Who Should Consider This Test
Individuals who exhibit symptoms such as jaundice, abdominal pain, or have a family history of hypercholanemia should consider this test. Additionally, those with risk factors for metabolic disorders are encouraged to undergo genetic testing to facilitate early diagnosis and management.
Benefits of Taking the Test
- Early detection of genetic predisposition to hypercholanemia.
- Informed decision-making regarding lifestyle and treatment options.
- Enhanced understanding of family health history and risks.
- Access to personalized medical advice and genetic counseling.
Understanding Your Results
Results from the BAAT Gene Hypercholanemia test will indicate whether genetic mutations are present. A genetic counselor will assist in interpreting these results, discussing their implications for health and potential preventive measures.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| BAAT Gene Hypercholanemia NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Now
Don’t wait to understand your genetic health! Book the BAAT Gene Hypercholanemia NGS Genetic DNA Test today for just 400,000 NGN. Contact us at +2348077798758 to schedule your appointment or for more information.
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 who is going for the BAAT Gene Hypercholanemia NGS Genetic DNA Test is required, along with a genetic counseling session to draw a pedigree chart of family members affected with hypercholanemia.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Metabolic Disorders
