Gilbert's syndrome and DNA diagnostics

DNA diagnosis of zilbera syndrome
DNA diagnosis of Gilbert's syndrome will help those who want to know a detailed picture of genetic abnormalities.

It is possible to enumerate deviations for a long time, at which DNA analysis can become a starting point for effective treatment. The modern possibilities of science are infinitely expanding. They help to put accurate diagnoses, helping to clarify the etymology of the disease at the DNA level. The DNA diagnosis of Gilbert's syndrome reveals the anomalous changes that have been formed, examines them and helps to determine the exact diagnosis.

The common man in the street does not know that there are a number of genetic diseases that are very similar in symptomatology, the course of the disease and the manifestation of distinctive features. Here, for example, syndromes Gilbert, Kriegler-Nayyar, Dabin-Johnson, Rotor, all viral hepatitis and hemolytic jaundice begin to flow almost identically. The patient experiences discomfort in the right hypochondrium, he has an appetite, he

quickly becomes tired, becomes irritable, listless, indifferent to the surrounding life. In many cases, a bright yellow color of the white coat of the eye is observed. A person realizes that he has got jaundice. But which one exactly?

Even an experienced doctor can not answer this question, so he prescribes certain tests, among which there will be DNA diagnostics of Gilbert Kriegler-Nayyar syndrome, Dabin-Johnson syndrome, Rotor. These types of diseases DNA diagnosis determines accurately, so a specialist can help a patient very quickly return to a full life.

Where it is possible to conduct DNA diagnosis of Gilbert's syndrome

The presence of the indicated disease may indicate the onset of a mutation of the UGT1A1 gene, which participates in the metabolism of bilirubin. As a result of a similar anomaly, there is a slight increase in the blood, which causes characteristic symptoms of jaundice.

But to be definitively confident in the diagnosis, it is necessary to conduct a complex study, such as DNA diagnostics. Gilbert's syndrome with it is determined with 100% accuracy. This method is safe, painless, fast and reliable. With its help, the frequency of repetitions in the promoter region of the designated gene is determined. This diagnosis is recommended to be performed before the treatment, before the use of drugs that have hepatotoxic effects.

DNA diagnosis, which determines the presence of Gilbert's syndrome, is conducted in specialized centers. The results are ready for the third day, so it will be possible to start treatment very quickly.

Procedure for DNA diagnosis of Gilbert's syndrome

To conduct DNA diagnostics capable of detecting mechanical jaundice( Gilbert's syndrome), it is necessary to get a referral from a geneticist who will compose a cover letter, in which the following information must be indicated:

  • patient's passport data;
  • address for sending the report;
  • enclosed a copy of the paid receipt.

The cost of analysis is indicated in the price list, which determines the services of the specialized center.

DNA analysis for mechanical jaundice will reveal conjugated hyperbilirubinemia, which is direct evidence of the presence of Gilbert's syndrome.

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