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Article

[Family study in Peutz-Jeghers syndrome].

Orvosi hetilap - 11 Feb 2007

Sarlós Patrícia, Király Agnes, Nagy Lajos

Abstract excerpt

BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant hereditary disease characterized by mucocutaneous pigmentation, gastrointestinal hamartomatous polyposis and an increased risk for the development of gastrointestinal and extra-gastrointestinal malignancies. AIM AND METHODS: Fi...

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Identifiers

PMID: 17344176
DOI: 10.1556/OH.2007.27640

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17344176-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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