Cronkhite–Canada syndrome: a report of two familial cases
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology
Link
http://link.springer.com/content/pdf/10.1007/s12664-012-0296-8.pdf
Reference7 articles.
1. Cronkhite LW Jr., Canada WJ. Generalized gastrointestinal polyposis: an unusual syndrome of polyposis, pigmentation, alopecia and onychotrophia. N Engl J Med. 1955;252:1011–5.
2. Riegert-Johnson DL, Osborn N, Smyrk T, Boardman LA. Cronkhite–Canada syndrome hamartomatous polyps are infiltrated with IgG4 plasma cells. Digestion. 2007;75:96–7.
3. Goto A. Cronkhite–Canada syndrome: epidemiological study of 110 cases reported in Japan. Nihon Geka Hokan. 1995;64:3–14.
4. Ward EM, Wolfsen HC. The non-inherited gastrointestinal polyposis syndromes. Aliment Pharmacol Ther. 2002;16:333–42.
5. Sampson JE, Harmon ML, Cushman M, Krawitt EL. Corticosteroid-responsive Cronkhite–Canada syndrome complicated by thrombosis. Dig Dis Sci. 2007;52:1137–40.
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4. Cronkhite-Canada syndrome: A case report and review of the literature;Annals of Medicine & Surgery;2022-09
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