Gilbert's syndrome in children

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

Gilbert's syndrome in children is an hereditary illness. It causes a number of serious violations in the blood, which increases the content of indirect bilirubin, which is the cause of jaundice. This syndrome is transmitted from parents to the child, it is well-studied and can be treated.

Gilbert's syndrome in children has characteristic signs that are easily detected in diagnosis. In the blood of the patient there is an increased content of bilirubin, a partial deficiency of glucuronyltransferase, a lack of functional changes in the liver, the presence of hereditary predisposition.

For the first time, the disease was described at the beginning of the XX century, numerous studies have shown that Gilbert's syndrome in children is most commonly found in males.

Gilbert's Syndrome: Symptoms and Diagnosis

The marked disease is most often diagnosed in adolescence: children begin to complain about aching pain and the unforeseen discomfort that occurs in the right hypochondrium. The child begins to get tired quickly, to become sluggish, and fatigue literally puts him at his feet. The main symptom pointing to intermittent jaundice in children is the bright-yellow color of the sclera of the organs of vision, it can then be manifested, then disappear, and all this will happen until the irritant factor is eliminated.

If you notice something similar to your child, contact your doctor urgently. He will assign the necessary tests to confirm or refute the previous diagnosis. The list of diagnostic procedures will necessarily include:



Gilbert's syndrome in children

Category Of Medical Issues: Diseases

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