Gilbert;s Syndrome Gene SequencingTest, Price, Normal Range | Sprint Diagnostics Hyderabad

Patient Preparing : No special preparation is required. However, inform your doctor of any medications you are taking.

₹ 7400

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.

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.

Test Name Gilbert's Syndrome Gene Sequencing (UGT1A1 Gene Polymorphism)
Sample Type Blood
Preparations Required No special preparation is required. However, inform your doctor of any medications you are taking.
Report Time 9 days
Price in Hyderabad ₹ 7400

What is Gilbert's Syndrome?

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.

What are the symptoms of Gilbert's Syndrome?

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

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How is Gilbert's Syndrome diagnosed?

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.

What is the UGT1A1 gene?

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.

How is Gilbert's Syndrome gene sequencing performed?

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.

Why is it important to get tested for 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.

Is there a cure for Gilbert's Syndrome?

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.

Can lifestyle changes help manage symptoms of Gilbert's Syndrome?

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

Should I be concerned if I am diagnosed with 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.

How common is Gilbert's Syndrome?

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

Is Gilbert's Syndrome hereditary?

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

Are there any medications that should be avoided by individuals with Gilbert's Syndrome?

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.

Can Gilbert's Syndrome affect routine blood tests?

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

Which doctor should be consulted in case of an abnormal result?

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.

Are there any complications associated with Gilbert's Syndrome?

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.

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