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A rare case of neonatal cholestasis
Journal article

A rare case of neonatal cholestasis

Abstract

A term appropriate for gestational age neonate presented with severe cholestasis with features of acute hepatic failure in early neonatal life. There was hypoglycemia, hyperammonemia, cholestasis, ascites, and hepatomegaly. Buccal mucosal biopsy containing minor salivary gland revealed iron deposition on Prussian blue staining suggestive of neonatal hemochromatosis. The neonate responded to exchange transfusion and intravenous immunoglobulin.

Authors

Ghoshal B; Das A; Mondal T

Journal

Journal of Clinical Neonatology, Vol. 6, No. 1, pp. 34–36

Publisher

Wolters Kluwer

Publication Date

2017

DOI

10.4103/2249-4847.199759

ISSN

2249-4847