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reduced results from
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873 B
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139 M
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18 M
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674
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601
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to
~98
options
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options split into images, definition, symptoms, related diagnoses, diagnostic tests, therapies, and medications
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gastrointestinal
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| frequency |
rare (U.S.)
Usually seen in those 50+.
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likelihood by age
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likelyhood by duration of symptoms
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Definition for
Cronkite-Canada Syndrome
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Cronkite-Canada Syndrome (CCS), first described in 1955, is a rare clinical syndrome of unknown etiology.
more
Cronkite-Canada Syndrome (CCS), first described in 1955, is a rare clinical syndrome of unknown etiology. CCS is diagnosed clinically, and the presenting symptoms include alopecia, cutaneous hyperpigmentation, gastrointestinal polyposis, and onychodystrophy, often accompanied by diarrhea, weight loss, and abdominal pain. We describe a unique case of CCS that presented with eosinophilic infilatrate on gastric and duodenal biopsies and review the literature pertaining to this rare syndrome.
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do i have 'Cronkite-Canada Syndrome'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
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diagnostic test search results for 'cronkite-canada syndrome'
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1 - 5 of 13 diagnostic tests
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therapeutic procedure search results for 'cronkite-canada syndrome'
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1 - 2 of 2 therapeutic procedures
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rankings are computer generated.
please consult your health care provider.
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medications search results for 'cronkite-canada syndrome'
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rankings are computer generated.
please consult your health care provider.
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