Gilbert's syndrome test

Gilbert’s syndrome test

This genetic test analyzes the presence of mutations in the UGT1A1 gene, specifically the UGT1A1*28 variant, which is responsible for the enzyme deficiency that characterizes Gilbert’s Syndrome.

199,00 €

Sample type saliva

Results delivery 4-6 weeks

Test DAO Kit delivered express worldwide

Gilbert’s syndrome test

199,00 €

Ingredientes saludables

What is Gilbert's Syndrome?

Gilbert’s syndrome is a benign genetic disorder that affects bilirubin metabolism in the liver. It is characterized by occasional episodes of mild jaundice (yellowing of the skin and eyes), especially during periods of stress, fasting, or intense exercise. Although it does not pose a serious health risk, knowing if you have the condition can help prevent misdiagnoses and allow for adjustments to medication regimens.

 

What should I keep in mind before taking the test?

No specific diet or guidelines should be followed prior to taking the test.

Test celiaquía DQ2/DQ8

Who is this test indicated for?

Individuals with elevated levels of unconjugated bilirubin without an apparent cause.
Patients with a family history of Gilbert’s syndrome.
People who experience mild jaundice recurrently.
Before starting treatments with medications metabolized by UGT1A1 (such as irinotecan).
Anyone who wishes to know their genetic predisposition.

Test sobrecrecimiento bacteriano - SIBO

Receive the kit at home, collect the samples following the instructions, and we will come to pick it up.

The kit will include detailed instructions on how to collect the sample and how to request a pickup.

Object of study

We evaluate the genetic predisposition to celiac disease

The celiac disease genetic predisposition test focuses on two specific genes: HLA-DQ2 and HLA-DQ8. Celiac disease is an autoimmune condition triggered by gluten ingestion in genetically susceptible individuals. The HLA-DQ2 and HLA-DQ8 genes encode histocompatibility proteins that play an important role in antigen presentation to immune system cells.

This test is used as a complementary diagnostic tool for people with symptoms of celiac disease. It can also be useful for first-degree relatives of patients with celiac disease to determine their genetic risk.

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— Our Commitment

Rigor, quality, and technology

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    Commitment to your digestive health

    At ADN Institut, we believe in a more proactive, personalized, and predictive approach to medicine. That's why our genetic tests not only offer a reliable diagnosis, but also allow us to anticipate potential health risks, improve the interpretation of symptoms, and tailor treatments to each individual.

  • Precision in genetic analysis

    Early detection of genetic conditions such as Gilbert's Syndrome is key to avoiding unnecessary treatments, optimizing drug response, and empowering the patient with valuable information about their health.

  • Personalized advice and professional support

    Because we understand that a genetic test must be accompanied by an appropriate clinical approach, at ADN Institut we offer the possibility of personalized medical or genetic counseling to help you interpret the results of your Gilbert's Syndrome test.

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