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Article

The Muir-Torre syndrome: a rare variant of hereditary nonpolyposis colorectal cancer associated with hMSH2 mutation.

The American journal of gastroenterology - 1 Sept 1998

Suspiro A, Fidalgo P, Cravo M, Albuquerque C, Ramalho E, Leitão C N, Costa Mira F

Abstract excerpt

The Muir-Torre syndrome is a rare autosomal dominant disorder characterized by the association of visceral malignancies with typical skin lesions. This syndrome is now considered a subtype of the more common hereditary nonpolyposis colorectal cancer syndrome (HNPCC). This last condition has been...

Topics

Colorectal Neoplasms, Hereditary Nonpolyposis
DNA-Binding Proteins
Female
Humans
Middle Aged
MutS Homolog 2 Protein
Neoplasm Proteins
Neoplasms, Multiple Primary
Phenotype
Proto-Oncogene Proteins
Skin Neoplasms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Syndrome

Source

Identifiers

PMID: 9732950
DOI: 10.1111/j.1572-0241.1998.00487.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9732950-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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The Muir-Torre syndrome: a rare variant of hereditary nonpolyposis colorectal cancer associated with hMSH2 mutation.PMID 9732950Read ↗

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Muir-Torre syndrome: case report and molecular characterization.Semantic proximity Read ↗

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