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Article

Cowden disease or multiple hamartoma syndrome--cutaneous clue to internal malignancy.

European journal of dermatology : EJD - 1 Jan 2000

Fistarol Susanna K, Anliker Marc D, Itin Peter H

Abstract excerpt

Cowden disease (CD) #158350, also known as multiple hamartoma syndrome, is a multisystemic cancer predisposition disorder, inherited in an autosomal dominant pattern. Mucocutaneous lesions are the most constant features: facial papules, acral keratoses and oral papillomatosis. The most common associated cancers are breast, thyroid and endometrial carcinomas. The CD gene locus has been mapped to chromosome...

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Source

Identifiers

PMID: 12370126

Genes

PTEN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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