Cronkhite-Canada syndrome (Q46733): Difference between revisions
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Síndrome de Cronkhite-Canadá (CCS) é um transtorno não hereditário de ocorrência esporádica de pólipos gastrointestinais generalizados (hamartomas), pigmentação cutânea, alopecia e onicodistrofia. A possibilidade de progressão para câncer é considerada baixa. Diarreia crônica e enteropatia perdedora de proteínas são frequentemente observadas. | |||
| description / en | description / en | ||
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. | |||
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. |
