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Article

A longitudinal study to identify laboratory predictors of liver disease outcome in Alagille syndrome.

Journal of pediatric gastroenterology and nutrition - 1 May 2010

Kamath Binita M, Munoz Pedro S, Bab Natalie, Baker Alastair, Chen Zhongxue, Spinner Nancy B, Piccoli David A

Abstract excerpt

OBJECTIVES: Liver disease in Alagille syndrome (AGS) is highly variable, ranging from biochemical abnormalities only to end-stage disease. It is not possible to predict whether a child with cholestasis will have improvement or progression of liver disease. This poses a challenge to the clinician in terms of timing therapies. The study aim was to identify laboratory markers present in children younger than 5 years...

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Identifiers

PMID: 20421762
DOI: 10.1097/MPG.0b013e3181cea48d
PMCID: PMC2861305

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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