Cronkhite-Canada syndrome

Cronkhite-Canada syndrome (CCS) is a rare gastrointestinal (GI) polyposis syndrome characterized by the association of non-hereditary GI polyposis with the cutaneous triad of alopecia, nail changes and hyperpigmentation.

Also known as: Cronkhite-Canada syndrome, gastric Cronkhite Canada polyposis, gastrointestinal polyposis-ectodermal changes syndrome, gastrointestinal polyposis-skin pigmentation-alopecia-fingernail changes syndrome, Cronkhite-Canada disease, polyposis skin pigmentation alopecia fingernail changes.

Category: General

Looking into Cronkhite-Canada syndrome? See the lab tests healthcare providers may use to investigate Cronkhite-Canada syndrome, and learn what each one measures.
Explore tests for Cronkhite-Canada syndrome
Symptoms

Symptoms associated with Cronkhite-Canada syndrome

The following symptoms have been associated with Cronkhite-Canada syndrome in medical literature. Not everyone experiences the same symptoms.

Tests

Tests used to investigate Cronkhite-Canada syndrome

Healthcare providers may order these tests when evaluating Cronkhite-Canada syndrome. Test selection is a clinical decision made by a qualified professional.

CBC with Differential

Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...

Sample: Blood

Comprehensive Metabolic Panel (CMP)

Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...

Sample: Blood

Urinalysis

Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....

Sample: Urine

Related conditions

Conditions with overlapping symptoms

These conditions share symptoms with Cronkhite-Canada syndrome, which is why a clinical evaluation is important.

FAQ

Frequently Asked Questions

What is Cronkhite-Canada syndrome?

Cronkhite-Canada syndrome is a health condition described in medical literature. Cronkhite-Canada syndrome (CCS) is a rare gastrointestinal (GI) polyposis syndrome characterized by the association of non-hereditary GI polyposis with the cutaneous triad of alopecia, nail changes and hyperpigmentation.

What are the symptoms of Cronkhite-Canada syndrome?

Cronkhite-Canada syndrome is associated with 7 symptoms in the medical literature we index, including Abdominal pain, Alopecia, Diarrhea, Hematochezia, Muscle weakness, Paresthesia. Symptoms vary widely between individuals.

How is Cronkhite-Canada syndrome diagnosed or investigated?

A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with Cronkhite-Canada syndrome include CBC with Differential, Comprehensive Metabolic Panel (CMP), Urinalysis. This information is educational, not a diagnosis.

Is SymptomDatabase.com diagnosing me?

No. SymptomDatabase.com does not provide diagnosis. If you are concerned you may have Cronkhite-Canada syndrome, please discuss your symptoms with a qualified healthcare provider.

Educational content only: The information on Symptom Database.com is for educational purposes and is not medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider. Read our full disclaimer.