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Disease Information for Multiple hamartoma syndrome

Clinical Manifestations

Signs & Symptoms

Cutaneous manifestations

Disease Progression

Course/Chronic disorder

Course/Chronic only

Demographics & Risk Factors

Population Group

Child

Population/Pediatrics population

Sex & Age Groups

Population/Child

Population/Child-Infant Only

Population/Children/all

Diagnostic Test Results

Other Tests & Procedures

Colonoscopy/Polyp

Associated Diseases & Rule outs

Associated Disease & Complications

Adenocarcinoma, breast

Multiple hamartoma syndrome

Thyroid Cancer

Thyroid malignancy/carcinoma

Thyroid papillary carcinoma

Disease Mechanism & Classification

Process

PROCESS/Benign tumor (ex).

PROCESS/Congenital/developmental (category)

PROCESS/Constitutional/essential disorder (ex)

PROCESS/Hamartoma type neoplasm (ex)

PROCESS/Hamartomatoses/Phakomatoses (ex)

PROCESS/Neoplastic (category)

PROCESS/Phakomatosis/congenital (ex)

PROCESS/Anomalies/Deformities/Malformations (EX)

PROCESS/Congenital neoplasm (ex)

Synonyms

Synonym

CD, COWDEN DIS, COWDEN DISEASE, Cowden syndrome, Cowden syndrome (disorder), COWDENS DIS, Cowdens Disease, Cowden's disease, Cowden's syndrome, CS, Disease Cowden, Disease Cowden's, Hamartoma Syndrome Multiple, MHAM, Multiple hamartoma syndrome, Syndrome Multiple Hamartoma, Synonym/Cowden's disease

Definition

A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Papules of the face and oral mucosa are the most characteristic lesion. Other changes occur in the skin, in the thyroid, the breast, the gastrointestinal system, and the nervous system.

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External Links Related to Multiple hamartoma syndrome

PubMed (National Library of Medicine)

NGC (National Guideline Clearinghouse)

Medscape (eMedicine)

Harrison's Online (accessmedicine)

NEJM (The New England Journal of Medicine)

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