Abstract
Background: Congenital hepatic fibrosis (CHF) is a rare developmental disorder caused by ductal plate malformation (DPM). So far, CHF has been described as a multiorgan disorder occurring in child- or young adulthood. In this study, we investigated 17 cases of CHF and their association with other diseases, gender distribution, age of clinical occurrence, form of clinical, morphological and laboratory presentation, long-term course and survival after transplantation.
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