| pubmed-article:17075480 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17075480 | lifeskim:mentions | umls-concept:C0439660 | lld:lifeskim |
| pubmed-article:17075480 | lifeskim:mentions | umls-concept:C0024623 | lld:lifeskim |
| pubmed-article:17075480 | lifeskim:mentions | umls-concept:C0205219 | lld:lifeskim |
| pubmed-article:17075480 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:17075480 | pubmed:dateCreated | 2006-10-31 | lld:pubmed |
| pubmed-article:17075480 | pubmed:abstractText | Some diffuse type gastric cancers are of hereditary origin. Their histological characteristics are poor cell differentiation and the presence of signet-ring cells. The cause is a mutation of the CDH1 gene which is responsible for abnormal E-cadherin. The transmission mode is autosomal dominant. Because of serious prognosis of symptomatic hereditary diffuse gastric cancer (HDGC), the high penetrance of the gene (67% in men and 83% in women) and the young age of onset of these tumors (before the age of 40), a prophylactic gastrectomy is recommended to the mutation carriers. The search for the genetic mutation should be recommended to families corresponding to clinical criteria such as the number of affected family members, degree of relationship and age of onset of these tumors. | lld:pubmed |
| pubmed-article:17075480 | pubmed:language | fre | lld:pubmed |
| pubmed-article:17075480 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17075480 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17075480 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17075480 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17075480 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:17075480 | pubmed:issn | 0399-8320 | lld:pubmed |
| pubmed-article:17075480 | pubmed:author | pubmed-author:LarueLionelL | lld:pubmed |
| pubmed-article:17075480 | pubmed:author | pubmed-author:FléjouJean-Fr... | lld:pubmed |
| pubmed-article:17075480 | pubmed:author | pubmed-author:SezeurAlainA | lld:pubmed |
| pubmed-article:17075480 | pubmed:author | pubmed-author:SchielkeAstri... | lld:pubmed |
| pubmed-article:17075480 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17075480 | pubmed:volume | 30 | lld:pubmed |
| pubmed-article:17075480 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17075480 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17075480 | pubmed:pagination | 1205-13 | lld:pubmed |
| pubmed-article:17075480 | pubmed:meshHeading | pubmed-meshheading:17075480... | lld:pubmed |
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| pubmed-article:17075480 | pubmed:meshHeading | pubmed-meshheading:17075480... | lld:pubmed |
| pubmed-article:17075480 | pubmed:meshHeading | pubmed-meshheading:17075480... | lld:pubmed |
| pubmed-article:17075480 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:17075480 | pubmed:articleTitle | [Hereditary diffuse gastric cancer]. | lld:pubmed |
| pubmed-article:17075480 | pubmed:affiliation | Service de Chirurgie digestive, Groupe Hospitalier Diaconesses-Croix Saint-Simon, Paris. asezeur@hopital-dcss.org <asezeur@hopital-dcss.org> | lld:pubmed |
| pubmed-article:17075480 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17075480 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:17075480 | pubmed:publicationType | English Abstract | lld:pubmed |
| pubmed-article:17075480 | pubmed:publicationType | Review | lld:pubmed |
