TJP2 Gene Hypercholanemia NGS Genetic DNA Test
Introduction
The TJP2 Gene Hypercholanemia NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with hypercholanemia, a metabolic disorder characterized by elevated bile acids in the bloodstream. This test employs Next-Generation Sequencing (NGS) technology to provide accurate and comprehensive insights into the genetic factors influencing bile acid metabolism.
What the Test Measures
This test specifically measures variations in the TJP2 gene, which plays a crucial role in bile acid transport and metabolism. By analyzing the genetic makeup of the patient, the test can detect mutations that may lead to hypercholanemia and other related metabolic disorders.
Who Should Consider This Test
Individuals who should consider the TJP2 Gene Hypercholanemia NGS Genetic DNA Test include:
- Patients exhibiting symptoms of hypercholanemia, such as jaundice, fatigue, and itching.
- Individuals with a family history of metabolic disorders.
- Patients who have been advised by a healthcare provider to undergo genetic testing for diagnostic purposes.
Benefits of Taking the Test
The TJP2 Gene Hypercholanemia NGS Genetic DNA Test offers several benefits:
- Early detection of genetic predispositions to hypercholanemia.
- Informed decision-making regarding treatment options.
- Enhanced understanding of the patient’s condition and potential risks.
- Guidance for family planning and genetic counseling.
Understanding Your Results
Once the test is completed, results will be provided with a comprehensive report. The report will include:
- Details of any detected mutations in the TJP2 gene.
- Interpretation of the results in relation to hypercholanemia.
- Recommendations for further testing or treatment options based on the findings.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| TJP2 Gene Hypercholanemia NGS Genetic DNA Test | KSh 40,000 | KSh 56,000 |
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or one drop of blood on an FTA card. Prior to testing, a clinical history of the patient and a genetic counseling session to draw a pedigree chart of affected family members are recommended.
Book Your Test Today!
We have branches across all major cities in Kenya, and we also offer home sample collection services for your convenience. To book the TJP2 Gene Hypercholanemia NGS Genetic DNA Test, please call or WhatsApp us at +254711564616. Take the first step towards understanding your health today!
