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 journalArticle

5 Citations (Scopus)

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 languageEnglish (US)
Pages (from-to)29-38
Number of pages10
JournalJournal of Radiology Case Reports
Volume6
Issue number2
DOIs
StatePublished - Feb 1 2012

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Cholestasis
Alagille Syndrome
Differential Diagnosis
Parturition

Keywords

  • Alagille syndrome
  • Biliary ducts
  • Cholestasis

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging

Cite this

Paucity of biliary ducts : A rare etiology of neonatal cholestasis. / Figiel, Steven Cornell; Franco, Arie; Pucar, Darko; Lewis, Kristopher Neal; Lee, Jeffrey Roberts.

In: Journal of Radiology Case Reports, Vol. 6, No. 2, 01.02.2012, p. 29-38.

Research output: Contribution to journalArticle

Figiel, Steven Cornell ; Franco, Arie ; Pucar, Darko ; Lewis, Kristopher Neal ; Lee, Jeffrey Roberts. / Paucity of biliary ducts : A rare etiology of neonatal cholestasis. In: Journal of Radiology Case Reports. 2012 ; Vol. 6, No. 2. pp. 29-38.
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