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Cronkhite-Canada syndrome: a report of two familial cases.
Indian J Gastroenterol
March 2013
Department of General Surgery, B.L.D.E.U.'s Shri B. M. Patil Medical College and Research Centre, Bijapur 586 103, India.
Cronkhite-Canada 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.
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