Genetics. PCR. Gilbert's syndrome (detection of UGT1A1 gene mutation)

Service description: Genetics. PCR. Gilbert's syndrome

Genetic research is a modern method that allows studying human genetic material in order to identify various mutations and hereditary diseases. One of the key services in this field is PCR– polymerase chain reaction, which provides accurate and rapid detection of specific DNA fragments.

What is Gilbert's syndrome?

Gilbert's syndrome is an inherited disorder characterized by a moderate increase in bilirubin levels in the blood, which can lead to jaundice. This disorder is caused by a mutation in the gene UGT1A1, which is responsible for bilirubin metabolism in the liver.

What is the purpose of our research?

Our gene mutation detection service UGT1A1 allows:

1. Make a diagnosis: Quickly and accurately detect mutations that cause Gilbert syndrome.
2. Predict risks: Assess the risk of developing complications and other diseases associated with dysfunction of bilirubin metabolism.
3. Optimize treatment: Provide doctors with accurate data to select optimal treatment and monitor the patient's condition.

How is the research conducted?

1. Material collection: A blood or saliva sample is taken for testing.
2. PCR: Using polymerase chain reaction, DNA fragments are isolated from the sample, which are then analyzed for the presence of mutations.
3. Analysis of results: The data obtained is processed, and the patient receives a detailed report on the results of the study.

Why choose us?

• High accuracy: Modern equipment and qualified specialists ensure high accuracy and reliability of results.
• Speed: We guarantee quick completion of the research and delivery of results.
• Privacy: All results and patient information are kept strictly confidential.

Study registration

If you suspect that you may have Gilbert syndrome, or if there are cases of this disease in your family, contact us to schedule a genetic test. Our team is ready to provide you with all the information and support you need.