Your Cart
Your cart is empty

Looks like you haven't added any test / checkup to your cart

Add Test / Checkup
User Sign In Health checkup offers
Lab Test

Gilbert's Syndrome Gene Sequencing (UGT1A1 Gene Polymorphism)

Gilbert's Syndrome is a common and mild liver disorder where the liver does not properly process bilirubin. Bilirubin is a yellow byproduct of the breakdown of old red blood cells. People with Gilbert's Syndrome often have elevated levels of bilirubin in the blood, which can cause the skin and eyes to occasionally turn yellow (jaundice). This syndrome is typically harmless and does not require treatment.

  • Test NameGilbert's Syndrome Gene Sequencing (UGT1A1 Gene Polymorphism)
  • Sample TypeBlood
  • Preparations RequiredNo special preparation is required. However, inform your doctor of any medications you are taking.
  • Report Time9 days

The underlying cause of Gilbert's Syndrome is a mutation in the UGT1A1 gene. This gene provides instructions for making an enzyme that helps break down bilirubin in the liver. When the gene is not working properly, bilirubin can build up in the blood. Gilbert's Syndrome Gene Sequencing involves analyzing the DNA of the UGT1A1 gene for mutations known to be associated with this syndrome.

Home Sample Collection Process

Book your convenient slot
Book your convenient slot
Sample Collection by Phlebotomist
Sample Collection by Phlebotomist
Reporting of the sample at lab
Reporting of the sample at lab
Download Reports
Download Reports
Frequently Asked Questions

Gilbert's Syndrome is a benign genetic liver condition in which the liver doesn't properly process bilirubin, leading to elevated levels of bilirubin in the blood and sometimes causing yellowing of the skin and eyes.

Many people with Gilbert's Syndrome experience no symptoms. When symptoms do occur, they often include mild jaundice, fatigue, and abdominal discomfort.

Diagnosis of Gilbert's Syndrome is usually made through blood tests that show elevated bilirubin levels. Genetic testing of the UGT1A1 gene can also be done to confirm the diagnosis.

The UGT1A1 gene provides instructions for making an enzyme that is involved in breaking down bilirubin in the liver. Mutations in this gene can impair the enzyme's function and lead to the buildup of bilirubin in the blood.

A blood sample is drawn from a vein in the arm. The DNA is extracted from the blood cells and the UGT1A1 gene is analyzed for mutations associated with Gilbert's Syndrome.

Testing for Gilbert's Syndrome is important for people who have unexplained elevated bilirubin levels or jaundice. Knowing that you have Gilbert's Syndrome can provide peace of mind as the condition is typically harmless.

There is no cure for Gilbert's Syndrome, but the condition is benign and typically does not require treatment. Managing stress and avoiding fasting or dehydration can help to reduce symptoms.

Yes, avoiding dehydration, eating regular meals, and managing stress can help to alleviate the symptoms of Gilbert's Syndrome.

Generally, Gilbert's Syndrome is a harmless condition. However, it's important to be aware of it because certain medications may affect bilirubin levels. Always inform your doctor if you have Gilbert's Syndrome before taking new medications.

Gilbert's Syndrome is relatively common. It affects about 3-12% of the population.

Yes, Gilbert's Syndrome is an inherited condition. It is passed down from parents to children through mutations in the UGT1A1 gene.

Individuals with Gilbert's Syndrome should be cautious with medications that can affect liver function or bilirubin levels. Consult your doctor before taking any new medication.

Yes, Gilbert's Syndrome can affect blood tests that measure liver function, as it may cause an increase in bilirubin levels.

If you are diagnosed with Gilbert's Syndrome or have abnormal results indicating elevated bilirubin levels, you should consult a hepatologist or a general physician.

Gilbert's Syndrome itself does not usually cause complications, but it's important to be aware of the condition, especially when taking medications that can affect the liver or bilirubin levels.

Gilbert's Syndrome is a mild genetic liver disorder characterized by elevated bilirubin levels. It's caused by mutations in the UGT1A1 gene. While the syndrome itself is usually harmless, it's important to be aware of it, especially regarding medication use and interpreting blood tests. If you suspect you may have Gilbert's Syndrome or have unexplained jaundice, consider speaking with your doctor about Gilbert's Syndrome Gene Sequencing.

Gilbert's Syndrome Gene Sequencing (UGT1A1 Gene Polymorphism)
₹ 7400 Add to Cart
Schedule Test in Your Available Time
Locations Near You in Hyderabad
  • 4KM from Madhapur
  • 3KM from Banjara Hills
  • 1.9KM from Yusufguda
  • 3KM from Madhura Nagar
  • 5KM from Shaikpet