| Literature DB >> 31335837 |
Krupa R Mysore1, Benjamin L Shneider, Sanjiv Harpavat.
Abstract
Biliary atresia (BA) is the most common reason for pediatric liver transplant. BA's varied presentation, natural history, and treatment with the Kasai portoenterostomy have been well described; however, when BA starts relative to birth has not been clearly defined. In this review, we discuss laboratory, imaging, and clinical data which suggest that most if not all forms of BA may start before birth. This early onset has implications in terms of delivering treatments earlier and identifying possible factors underlying BA's etiology.Entities:
Year: 2019 PMID: 31335837 PMCID: PMC6942669 DOI: 10.1097/MPG.0000000000002450
Source DB: PubMed Journal: J Pediatr Gastroenterol Nutr ISSN: 0277-2116 Impact factor: 2.839