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Article

A genotype-phenotype correlation in HNPCC: strong predominance of <i>msh2</i> mutations in 41 patients with Muir-Torre syndrome

1 Jul 2004

Abstract excerpt

Muir-Torre syndrome (MTS; MIM 158320) is an autosomal dominant predisposition to skin tumours and various internal malignancies. Clinical criteria for a diagnosis of MTS are the synchronous or metachronous occurrence of at least one sebaceous gland neoplasia and at least one internal neoplasm in a patient (regardless of the family history).1,2 The sebaceous gland neoplasias comprise adenomas, epitheliomas...

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Identifiers

PMID: 15235030
DOI: 10.1136/jmg.2003.012997

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A genotype-phenotype correlation in HNPCC: strong predominance of <i>msh2</i> mutations in 41 patients with Muir-Torre syndromePMID 15235030Read ↗

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