Table of Contents Author Guidelines Submit a Manuscript
Case Reports in Gastrointestinal Medicine
Volume 2015, Article ID 140616, 5 pages
http://dx.doi.org/10.1155/2015/140616
Case Report

A Novel SMAD4 Mutation Causing Severe Juvenile Polyposis Syndrome with Protein Losing Enteropathy, Immunodeficiency, and Hereditary Haemorrhagic Telangiectasia

1Gastroenterology and Hepatology Unit, Department of Clinical and Experimental Medicine, Faculty of Health Sciences, Linköping University, County Council of Östergötland, 581 85 Linköping, Sweden
2Department of Clinical Pathology and Clinical Genetics and Department of Clinical and Experimental Medicine, Faculty of Health Sciences, Linköping University, County Council of Östergötland, 581 85 Linköping, Sweden
3Division of Infectious Diseases, Department of Clinical and Experimental Medicine, Faculty of Health Sciences, Linköping University, County Council of Östergötland, 581 85 Linköping, Sweden
4Department of Clinical Pathology and Genetics, Sahlgrenska University Hospital, 413 45 Gothenburg, Sweden

Received 29 October 2014; Revised 16 January 2015; Accepted 20 January 2015

Academic Editor: Yoshifumi Nakayama

Copyright © 2015 Joel Johansson et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Joel Johansson, Christofer Sahin, Rebecka Pestoff, et al., “A Novel SMAD4 Mutation Causing Severe Juvenile Polyposis Syndrome with Protein Losing Enteropathy, Immunodeficiency, and Hereditary Haemorrhagic Telangiectasia,” Case Reports in Gastrointestinal Medicine, vol. 2015, Article ID 140616, 5 pages, 2015. https://doi.org/10.1155/2015/140616.