Cronkhite-Canada Syndrome

Overview

A nonfamilial polyposis syndrome that is characterized by the presence of diffuse gastrointestinal polyposis, skin hyperpigmentation, ALOPECIA; DIARRHEA, and PROTEIN-LOSING ENTEROPATHY. It was first reported by Cronkhite and Canada in 1955.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Cronkhite-Canada Syndrome

Topic type

Condition

Category

Dermatology

MeSH classification

C06.405.469.578.500|C17.800.621.340|C23.550.755.500

Preparing for an appointment about Cronkhite-Canada Syndrome

If you are speaking with a healthcare professional about Cronkhite-Canada Syndrome, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

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