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Syndromic (phenotypic) diarrhea in early infancy

Olivier Goulet1 email, Christine Vinson2 email, Bertrand Roquelaure3 email, Nicole Brousse4 email, Christine Bodemer5 email and Jean-Pierre Cézard2 email

Pediatric Gastroenterology-Hepatology and Nutrition, Reference Center for Rare Digestive Disease, Hôpital Necker-Enfants Malades/AP-HP, University of Paris 5 – René Descartes, France

Pediatric Gastroenterology and Nutrition, Reference Center for Rare Digestive Disease, Hôpital Robert Debré/AP-HP, University of Paris 7, France

Pediatric Gastroenterology and Nutrition, Hôpital de la Timone, University of Marseille, France

Department of Pathology, Hôpital Necker-Enfants Malades/AP-HP, University of Paris 5 – René Descartes, France

Pediatric Dermatology, Reference Center for Rare Dermatologic Disease, Hôpital Necker-Enfants Malades/AP-HP, University of Paris 5 – René Descartes, France

author email corresponding author email

Orphanet Journal of Rare Diseases 2008, 3:6doi:10.1186/1750-1172-3-6

Published: 28 February 2008

Additional files

Additional file 1:

Clinical features in patients with Syndromic (phenotypic) diarrhea. This table includes data from the published cases in the literature (patients 1–17, References 9–15). Patients 18 to 25 are currently under publication by the authors.

Format: DOC Size: 65KB Download file

This file can be viewed with: Microsoft Word Viewer


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