A case of Cronkhite-Canada syndrome with taste disturbance as a leading complaint.

Wojciech C Blonski, Emma E Furth, Bruce P Kinosian, Charlene Compher, David C Metz

Journal: Digestion 2005;71(4):201-5

PMID: 15942207

Abstract

Cronkhite-Canada syndrome was first described in 1955. The clinical features of this rare syndrome of unknown etiology include nonhereditary gastrointestinal polyposis together with diarrhea, nail dystrophy, alopecia, and hyperpigmentation of the skin. This syndrome has been divided into five clinical types based on initial symptoms. We describe a case of Cronkhite-Canada syndrome presenting with taste disturbance as the major symptom, present a comprehensive review of the literature concerning this rare syndrome, and suggest therapeutic treatment options.

Copyright (c) 2005 S. Karger AG, Basel.

Address: Division of Gastroenterology, University of Pennsylvania Health System, Philadelphia, Pa. 19104, USA.

Link outs

Subscription / membership required

Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.