UGT1A1 Gene Gilbert Syndrome NGS Genetic DNA Test
Introduction to the UGT1A1 Gene Gilbert Syndrome NGS Genetic DNA Test
The UGT1A1 Gene Gilbert Syndrome NGS Genetic DNA Test is a crucial diagnostic tool that helps in the identification of genetic variations associated with Gilbert syndrome. This condition, characterized by elevated levels of bilirubin in the blood, can lead to jaundice and other liver-related issues. Understanding your genetic predisposition through this test is vital for early intervention and management.
What the Test Measures
This test specifically measures variations in the UGT1A1 gene, which is responsible for bilirubin metabolism. By utilizing Next-Generation Sequencing (NGS) technology, the test provides comprehensive insights into the genetic factors that may contribute to Gilbert syndrome.
Who Should Consider This Test
Individuals who exhibit symptoms such as unexplained jaundice, fatigue, or have a family history of liver disorders should consider the UGT1A1 Gene Gilbert Syndrome NGS Genetic DNA Test. Additionally, those with risk factors for hepatology, nephrology, or endocrinology disorders may benefit from this genetic evaluation.
Benefits of Taking the Test
- Identifies genetic predispositions to Gilbert syndrome.
- Facilitates personalized treatment plans based on genetic insights.
- Provides peace of mind for individuals with a family history of the condition.
- Helps in making informed decisions regarding health management.
Understanding Your Results
Upon completion of the test, results will indicate whether any genetic variations associated with Gilbert syndrome are present. It is essential to discuss these results with a healthcare professional to understand their implications fully and to determine the best course of action.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the UGT1A1 Gene Gilbert Syndrome NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and answer any questions you may have.
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical history of the patient who is going for the test, along with a genetic counseling session to draw a pedigree chart of family members affected by the UGT1A1 gene.
This test falls under the specialty of General Physician and the department of Genetics, focusing on Hepatology, Nephrology, and Endocrinology disorders.
