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, hequickly 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.
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.
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:
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.
Some people, especially in children, there is a constant hiccups after eating.This is due to many different factors: the poor assimilation of fo...
This unpleasant problem as diarrhea after eating can have various causes.In any case it is necessary to find out the essence of the disease, and...
Due to its physical and chemical properties of beryllium in demand in the industry.However, beryllium is highly toxic - it causes beryllium lung...