Cronkhite-Canada syndrome (Q46733): Difference between revisions
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Revision as of 15:32, 13 August 2026
Cronkhite-Canada syndrome (CCS) is a sporadically occurring, noninherited disorder of generalised gastrointestinal polyps (hamartomas), cutaneous pigmentation, alopecia, and onychodystrophy. The possibility of progression to cancer is considered to be low. Chronic diarrhea and protein-losing enteropathy are often observed.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD27.01 |
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| English | Cronkhite-Canada syndrome |
Cronkhite-Canada syndrome (CCS) is a sporadically occurring, noninherited disorder of generalised gastrointestinal polyps (hamartomas), cutaneous pigmentation, alopecia, and onychodystrophy. The possibility of progression to cancer is considered to be low. Chronic diarrhea and protein-losing enteropathy are often observed. |
Statements
CID11:LD27.01
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dki-india-LD27.01
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