| Literature DB >> 6714066 |
A G Peart, M V Sivak, G B Rankin, L S Kish, W D Steck.
Abstract
A case report of a 34-year-old female with the Cronkhite-Canada syndrome is presented. The patient developed the characteristic clinical features of intestinal polyposis, skin pigmentation, alopecia, and onychodystrophy which later resolved. An unusual feature was that symptoms developed during the postpartum period. This is the youngest female patient described with the syndrome. The etiology, pathophysiology, clinical manifestations, and management of the Cronkhite-Canada syndrome are reviewed.Entities:
Mesh:
Year: 1984 PMID: 6714066 DOI: 10.1007/bf01296227
Source DB: PubMed Journal: Dig Dis Sci ISSN: 0163-2116 Impact factor: 3.199