Gilbert's syndrome: bilirubin level

Gilbert'S Syndrome (Health And Medical Video July 2018).

Gilbert's syndrome, bilirubin have cause-and-effect relationships. Gilbert's syndrome appears precisely because of this special bile enzyme, which as a result of genetically determined deficiency in the liver cells is altered, transforming from indirect bilirubin into a direct one.

Today in medicine 2 types of bilirubin are allocated: direct and indirect. Indirect bilirubin, passing through the liver, is affected by glucuronic acid decomposed and excreted from the body. But if the body undergoes severe hormonal malfunctioning, indirect bilirubin begins to accumulate in the liver, which does not have time to process it. In this case, the bile ferment paints the skin and mucous organs of the eyes in a bright yellow color, indicating that the usual jaundice began.

Similar crashes can occur at the genetic level, then the extremely clear diagnosis - Gilbert's syndrome. Bilirubin in this disease does not pass the stage of usual processing due to lack of enzyme glucuronyltransferase. The person has the characteristic symptoms:

  • Severe headaches;
  • Weakness and fatigue;
  • Minor pains in the right hypochondrium;
  • Nausea and bitterness in the mouth.

Gilbert's syndrome, or pigmented hepatosis, is not a disease, but a special condition characterized by a constantly high level of bilirubin in the blood, but it can be diagnosed only after DNA analysis, which eliminates similar diseases.

Gilbert's syndrome: diagnostic methods that show elevated levels of bilirubin

There are special diseases that accompany a person throughout his life, among others stands out Gilbert's syndrome. Bilirubin, its amount in the blood indicates the stage of the course of the disease, therefore, among other diagnostic methods, the biochemical blood test is considered to be the simplest and most effective method, which gives the physician the opportunity to orientate in the clinical picture.

In addition, the patient is always advised to undergo genetic testing, which can 100% confirm the marked diagnosis. Few people know that there are a lot of similar diseases that have the same symptoms, therefore it is not possible to talk about genetic jaundice only at an elevated level of the bile enzyme.

If you suspect Gilbert syndrome, the doctor will definitely prescribe duodenal sensation and liver biopsy. Experts will tell all the features of diagnosis and determine the strategy of treatment.

Increased bilirubin in Gilbert syndrome: treatment methods

It is easy to reduce bilirubin levels. Treatment is selected individually, but, as a rule, it is reduced to choosing the right diet, limiting physical activity, taking multivitamin complexes and choleretic drugs. However, neglecting the help of a specialist is not worthwhile, as should not be engaged in and dangerous self-medication.

Remember: you do not need to panic. Modern medicine is quite capable of helping those who have been diagnosed with Gilbert's syndrome. Bilirubin, its level, all internal processes is an opportunity to control, helping patients improve their quality of life.

Gilbert's syndrome: bilirubin level

Category Of Medical Issues: Diseases

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