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Updated: Aug 1, 2026

Isolation of Neonatal Extrahepatic Cholangiocytes
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Síndrome de Gilbert y hiperbilirrubinaemia en recién nacidos incompatibles con ABO

M Kaplan, C Hammerman, P Renbaum

    Lancet (London, England)
    |September 1, 2000
    PubMed
    Resumen

    El síndrome de Gilbert, un polimorfismo promotor del gen UGT, aumenta significativamente el riesgo de hiperbilirrubinemia neonatal en los bebés directos de Coombs negativos a la ABO. Este factor genético es crucial para comprender la ictericia severa en estos recién nacidos.

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