Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome.

The aim of this work was to evaluate the influence of abnormal UDP-glucoronosyltransferase-1 (UGT1A1) gene variant, on the incidence and severity of neonatal hyperbilirubinemia, in glucose-6-phosphate dehydrogenase (G6PD) deficient newborns. The A(TA)nTAA region in the promoter of the UGT1A1 gene wa...

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Bibliographic Details
Main Author: Costa, Elísio (author)
Other Authors: Vieira, Emilia (author), Cleto, Esmeralda (author), Cabeda, José M (author), Pinho, Luciana (author), Coimbra, Eduarda (author), Dos Santos, Rosário (author), Barbot, José (author)
Format: article
Language:por
Published: 2002
Online Access:https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1986
Country:Portugal
Oai:oai:ojs.www.actamedicaportuguesa.com:article/1986

Internet

https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1986

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