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GILBERT'S SYNDROME IN CHILDREN: CONTEMPORARY DIAGNOSTIC POTENTIALITIES

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Gilbert's syndrome is a benign indirect hyperbilirubinemia of the hereditary nature, caused by deficiency of the enzyme uridindiphosphatglucuronitransferase. UGT1A1 gene is localized on chromosome 2q37. The most common is a defect in the promoter region of the gene pairs in the thymine-adenin....

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Main Authors: I.N. Zakharova (Author), M.I. Pykov (Author), Z.V. Kaloeva (Author), L.A. Kataeva (Author), S.V. Shishkina (Author), I.V. Berezhnaya (Author), E.V. Reznichenko (Author), N.V. Molotkova (Author)
Format: Book
Published: Union of pediatricians of Russia, 2011-08-01T00:00:00Z.
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