Cronkhite - Canada syndrome: a report of two familial cases

Patil V, Patil LS Jakareddy R Verma A  Gupta AB

dc.contributor.author	Patil V, Patil LS Jakareddy R Verma A Gupta AB
dc.date.accessioned	2020-01-14T05:04:29Z
dc.date.available	2020-01-14T05:04:29Z
dc.date.issued	2013-03
dc.identifier.uri	http://hdl.handle.net/123456789/1699
dc.description.abstract	CronkhiteCanada syndrome (CCS) is a rare syndrome first described in 1955. Since then, over 400 cases worldwide have been reported in the literature. The disease is characterized by diffuse gastrointestinal polyposis, dystrophic changes of the fingernails, alopecia, cutaneous hyperpigmentation, diarrhea, weight loss, and abdominal pain. An autoimmune etiology is suspected. The workup is based on history and physical examination,	en_US
dc.language.iso	en	en_US
dc.publisher	BLDE(Deemed to be University)	en_US
dc.subject	CronkhiteCanada syndrome (CCS) is a rare syndrome first described in 1955	en_US
dc.title	Cronkhite - Canada syndrome: a report of two familial cases	en_US
dc.type	Article	en_US