rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
8-9
|
pubmed:dateCreated |
1999-11-9
|
pubmed:abstractText |
The Muir-Torre syndrome is an autosomal dominant hereditary condition predisposing to cancer. It is characterized by skin tumors associated with adenocarcinoma of the colon or other neoplasias observed in the context of hereditary non-polyposis colorectal cancer (HNPCC). The Muir-Torre syndrome is also characterized by the frequent presence of multiple colonic polyps and the relatively moderate aggressivity of the tumors.
|
pubmed:commentsCorrections |
|
pubmed:language |
fre
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0151-9638
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
126
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
600-3
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:10530347-Adenocarcinoma,
pubmed-meshheading:10530347-Adenosine Triphosphatases,
pubmed-meshheading:10530347-Aged,
pubmed-meshheading:10530347-Base Pair Mismatch,
pubmed-meshheading:10530347-Codon,
pubmed-meshheading:10530347-Colonic Neoplasms,
pubmed-meshheading:10530347-Colonic Polyps,
pubmed-meshheading:10530347-Colorectal Neoplasms, Hereditary Nonpolyposis,
pubmed-meshheading:10530347-DNA-Binding Proteins,
pubmed-meshheading:10530347-Exons,
pubmed-meshheading:10530347-Female,
pubmed-meshheading:10530347-Gastrointestinal Neoplasms,
pubmed-meshheading:10530347-Genes, Dominant,
pubmed-meshheading:10530347-Germ-Line Mutation,
pubmed-meshheading:10530347-Guanine,
pubmed-meshheading:10530347-Heterozygote,
pubmed-meshheading:10530347-Humans,
pubmed-meshheading:10530347-Keratoacanthoma,
pubmed-meshheading:10530347-MutS Homolog 2 Protein,
pubmed-meshheading:10530347-Mutagenesis, Insertional,
pubmed-meshheading:10530347-Proto-Oncogene Proteins,
pubmed-meshheading:10530347-Risk Factors,
pubmed-meshheading:10530347-Sebaceous Gland Neoplasms,
pubmed-meshheading:10530347-Skin Neoplasms,
pubmed-meshheading:10530347-Syndrome
|
pubmed:articleTitle |
[Mutation in the MSH2 gene in Muir-Torre syndrome].
|
pubmed:affiliation |
Laboratoire de Génétique Moléculaire, Hôpital Tenon, Paris.
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports,
Research Support, Non-U.S. Gov't
|