Paucity of biliary ducts: A rare etiology of neonatal cholestasis

Steven Cornell Figiel; Arie Franco; Darko Pucar; Kristopher Neal Lewis; Jeffrey Roberts Lee

doi:10.3941/jrcr.v6i2.892

Paucity of biliary ducts: A rare etiology of neonatal cholestasis

Steven Cornell Figiel, Arie Franco, Darko Pucar, Kristopher Neal Lewis, Jeffrey Roberts Lee

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Abstract

We report a case of a newborn with cholestasis that was diagnosed as nonsyndromic Alagille syndrome. The main feature of the disease is a paucity of biliary ducts. There are two known types of the disease: the syndromic type which is associated with other congenital defects and the nonsyndromic type without other anomalies detected at birth. We describe the case and discuss its clinical and radiologic findings. We also discuss the various etiologies of cholestasis that are included in the differential diagnosis.

Original language	English (US)
Pages (from-to)	29-38
Number of pages	10
Journal	Journal of Radiology Case Reports
Volume	6
Issue number	2
DOIs	https://doi.org/10.3941/jrcr.v6i2.892
State	Published - Feb 2012

Keywords

Alagille syndrome
Biliary ducts
Cholestasis

ASJC Scopus subject areas

Radiology Nuclear Medicine and imaging

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abstract = "We report a case of a newborn with cholestasis that was diagnosed as nonsyndromic Alagille syndrome. The main feature of the disease is a paucity of biliary ducts. There are two known types of the disease: the syndromic type which is associated with other congenital defects and the nonsyndromic type without other anomalies detected at birth. We describe the case and discuss its clinical and radiologic findings. We also discuss the various etiologies of cholestasis that are included in the differential diagnosis.",

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AU - Franco, Arie

AU - Pucar, Darko

AU - Lewis, Kristopher Neal

AU - Lee, Jeffrey Roberts

PY - 2012/2

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N2 - We report a case of a newborn with cholestasis that was diagnosed as nonsyndromic Alagille syndrome. The main feature of the disease is a paucity of biliary ducts. There are two known types of the disease: the syndromic type which is associated with other congenital defects and the nonsyndromic type without other anomalies detected at birth. We describe the case and discuss its clinical and radiologic findings. We also discuss the various etiologies of cholestasis that are included in the differential diagnosis.

AB - We report a case of a newborn with cholestasis that was diagnosed as nonsyndromic Alagille syndrome. The main feature of the disease is a paucity of biliary ducts. There are two known types of the disease: the syndromic type which is associated with other congenital defects and the nonsyndromic type without other anomalies detected at birth. We describe the case and discuss its clinical and radiologic findings. We also discuss the various etiologies of cholestasis that are included in the differential diagnosis.

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KW - Biliary ducts

KW - Cholestasis

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Paucity of biliary ducts: A rare etiology of neonatal cholestasis

Abstract

Keywords

ASJC Scopus subject areas

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