Cronkhite-Canada syndrome (Q46733): Difference between revisions

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CID11:LD27.01
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dki-india-LD27.01
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Concluído
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
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CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10: FLAVIA MARIA DOS SANTOS BERGAMI / rank
 
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Latest 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
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LD27.01
    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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      Concluído
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      13 August 2026
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