Results 111 to 120 of about 510 (145)
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The Journal of the Association of Physicians of India, 2001
Cronkhite Canada syndrome is an acquired non-familial syndrome characterised by diffuse gastrointestinal polyposis with alopecia nail dystrophy and hyperpigmentation. There is chronic diarrhoea and protein losing enteropathy. The etiology of this syndrome remains obscure. The rarity of the case prompts this case report.
A, Sood, N, Sood, V, Midha
openaire +1 more source
Cronkhite Canada syndrome is an acquired non-familial syndrome characterised by diffuse gastrointestinal polyposis with alopecia nail dystrophy and hyperpigmentation. There is chronic diarrhoea and protein losing enteropathy. The etiology of this syndrome remains obscure. The rarity of the case prompts this case report.
A, Sood, N, Sood, V, Midha
openaire +1 more source
Gastroenterologia y hepatologia, 1998
The case of a 76-year-old patient with the Cronkhite-Canada syndrome admitted for diarrhea is presented. Although the clinical, endoscopical and histological data suggested the diagnosis, confirmation was achieved following necropsy, as well the evolution and the different treatment schedules carried out.
C, Muñoz +4 more
openaire +1 more source
The case of a 76-year-old patient with the Cronkhite-Canada syndrome admitted for diarrhea is presented. Although the clinical, endoscopical and histological data suggested the diagnosis, confirmation was achieved following necropsy, as well the evolution and the different treatment schedules carried out.
C, Muñoz +4 more
openaire +1 more source
Gastrointestinal: Cronkhite‐Canada syndrome
Journal of Gastroenterology and Hepatology, 1998A J, Wigg +2 more
openaire +2 more sources
Alopecia in Cronkhite-Canada syndrome
British Journal of Dermatology, 2017C, Stefanaki, A, Stratigos
openaire +2 more sources
Cronkhite-Canada syndrome: a retrospective analysis of four cases at a single medical center
Scandinavian Journal of Gastroenterology, 2022Chengdang Wang, Long Chen
exaly

