Secondary Logo

Institutional members access full text with Ovid®

A Rare Case Of a 2-year-old Boy With Alagille Syndrome and Type 3 Hereditary Hemochromatosis With TFR2 Mutation

Khayat, Ammar A.*; Suchi, Mariko; Vitola, Bernadette*

Journal of Pediatric Gastroenterology and Nutrition: April 2019 - Volume 68 - Issue 4 - p e68–e70
doi: 10.1097/MPG.0000000000002078
Case Report

*Pediatric Gastroenterology

Pathology, Medical College of Wisconsin, Milwaukee, WI.

Address correspondence and reprint requests to Ammar A. Khayat, MD, Medical College of Wisconsin, Pediatric Gastroenterology, 8701 Watertown Plank Road, Milwaukee, WI 53226 (e-mail:

Received 3 March, 2018

Accepted 11 May, 2018

Supplemental digital content is available for this article. Direct URL citations appear in the printed text, and links to the digital files are provided in the HTML text of this article on the journal's Web site (

The authors report no conflicts of interest.

© 2019 by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology,