WebSchlu¨sselwo¨rter: Cronkhite-Canada-Syndrom – nicht familia¨re Polyposis – juvenile Polyposis – p53 – c-erbB 2. Definition 1955 wurde erstmals von Cronkhite und Canada das Syndrom der sog. „nicht familia¨ren Polyposis“ beschrie-ben, bei dem zahlreiche (juvenile) Polypen des Gastro-intestinaltrakts mit Haut- und Nagelvera ... Web一站式科研服务平台. 学术工具. 文档翻译; 收录引证; 论文查重; 文档转换
Familial adenomatous polyposis - Wikipedia
WebApr 10, 2024 · Cronkhite-Canada syndrome (CCS) is an extremely rare disease characterized by various intestinal polyps, loss of taste, hair loss, and nail growth problems. It is difficult to treat because of malabsorption that accompanies the polyps. CCS occurs … WebCronkhite-Canada syndrome (Q1422034) Cronkhite-Canada syndrome. syndrome characterized by multiple polyps of the digestive tract. gastric Cronkhite Canada polyposis. Cronkhite–Canada syndrome. polyposis, skin pigmentation, alopecia, and fingernail changes. Cronkhite-Canada Syndrome. island iv form
Cronkhite-Canada Syndrome - Symptoms, Causes, …
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), and it is currently considered acquired and idiopathic (i.e. cause remains unknown). About two-thirds of patients are of Japanese descent and the male to female ratio is 3:2. It was characterized in 1955 by internal medicine physician Leonard Wolsey Cronkhite Jr. and radiolog… WebOct 4, 2024 · Cronkhite-Canada syndrome (CCS) is a rare acquired polyposis with unknown etiology. To date, >500 cases have been reported worldwide. CCS is typically … WebInterestingly, among patients with CCS a significant correlation (16.5 %) with intestinal carcinomas has been observed, suggesting malignant transformation and/or genetic predisposition may be involved in the initiation of the disease. Summary. Juvenile polyposis was first described by Cronkhite and Canada in 1955. This disease is characterized by … keystone ccc