Direct Hyperbilirubinemia in an Infant

Abstract

Get full access to this article

View all access options for this article.

References

Lauer

Spector

ND.

Hyperbilirubinemia in the newborn. Pediatr Rev. 2011;32:341-349.

Alagille

Odievre

Gautier

Dommergues

JP.

Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur. J Pediatr. 1975;86:63-71.

Brumbaugh

Mack

Conjugated hyperbilirubinemia in children. Pediatr Rev. 2012;33:291-302.

Ahn

Yoon

Kim

. Alagille syndrome and a JAG1 mutation: 41 cases of experience at a single center. Korean J Pediatr. 2015;58:392-397.

Grochowski

Loomes

Spinner

NB.

Jagged1 (JAG1): structure, expression, and disease associations. Gene. 2016;576(1 pt 3):381-384.

Emerick

Rand

Goldmuntz

Krantz

Spinner

Piccoli

DA.

Features of Alagille syndrome in 92 patients: frequency and relation to prognosis. Hepatology. 1999;29:822-829.

Prescilla

Lin

. Index of suspicion. Case 1. Alagille syndrome. Pediatr Rev. 1999;20:309-310.

Hartley

Gissen

Kelly

DA.

Alagille syndrome and other hereditary causes of cholestasis. Clin Liver Dis. 2013;17:279-300.

D’Agata

Balistreri

WF.

Evaluation of liver disease in the pediatric patient. Pediatr Rev. 1999;20:376-390.

10.

Hingorani

Nischal

Davies

. Ocular abnormalities in Alagille syndrome. Ophthalmology. 1999;106:330-337.

11.

Lykavieris

Hadchouel

Chardot

Bernard

Outcome of liver disease in children with Alagille syndrome: a study of 163 patients. Gut. 2001;49:431-435.