Cronkhite-Canada

Cronkhite–Canada syndrome: from clinical features to …

Cronkhite–Canada syndrome - Wikipedia

Cronkhite–Canada syndrome is a rare syndrome characterized by multiple polyps of the digestive tract. It is sporadic (i.e. it does not seem to be a hereditary disease), [1] and it is currently considered …

Cronkhite-Canada综合征发病机制及临床诊治研究进展

Cronkhite-Canada 综合征（CCS）是一种以胃肠道多发息肉和外胚层改变为特征的罕见疾病，又名胃肠道息肉-色素沉着-脱发-指（趾）甲营养不良综合征。 其病因尚未完全阐明，目前以免疫抑制治疗（ …

Cronkhite-Canada syndrome: A case report and review of the …

2022年9月1日 · 1. Introduction Cronkhite-Canada syndrome (CCS) is a rare, non-hereditary disease characterized by multiple polyps and ectodermal changes in the gastrointestinal tract, also known as …

Cronkhite-Canada Syndrome - Clinical Gastroenterology and Hepatology

2021年9月4日 · Cronkhite-Canada syndrome is an extremely rare, noninherited condition associated with widespread gastrointestinal polyps, alopecia, onychodystrophy, skin hyperpigmentation, and …

Cronkhite-Canada syndrome - Orphanet

Cronkhite-Canada syndrome (CCS) is a rare gastrointestinal (GI) polyposis syndrome characterized by the association of non-hereditary GI polyposis with the cutaneous triad of alopecia, nail changes and …

Case Report: Cronkhite-Canada syndrome: …

Cronkhite–Canada syndrome - DermNet

Cronkhite-Canada syndrome: from clinical features to treatment

2020年10月4日 · Cronkhite-Canada syndrome (CCS) is a rare acquired polyposis with unknown etiology. To date, >500 cases have been reported worldwide. CCS is typically characterized by …