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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2001-3-15
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pubmed:abstractText |
Familial adenomatous polyposis (FAP) is characterised by the presence of profuse colonic carpeting of adenomas throughout the entire colon and rectum. The genetic basis of FAP has been shown to be primarily associated with germline mutations in the APC gene. Notwithstanding, several reports have been published indicating that there is genetic heterogeneity in FAP and that the most likely explanation is the existence of another gene. In this report we further delineate the genotype/phenotype correlation in families that harbour germline mutations in the APC gene and identify some previously unreported changes in the APC gene which predispose to an attenuated disease phenotype. From 53 index patients diagnosed with either FAP or attenuated FAP, 27 harboured changes in the APC gene. The remaining 26 patients were further subgrouped according to their colonic phenotype. There were nine patients with a mixed hyperplastic/adenomatous colonic phenotype and there were 17 patients with an adenomatous colonic phenotype. Evaluation of the disease characteristics of these patients and their families is presented which may aid in the identification of new genes associated with colonic polyposis.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-10235578,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-10346819,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-1651174,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-1651562,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-1651563,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-1678319,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-1968211,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-3039373,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-3340553,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-3789010,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-7606712,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-7741978,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-7749328,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-7795585,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-7797123,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-7833149,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8111410,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8199599,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8247073,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8252630,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8256823,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8385563,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8625064,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8638125,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8730280,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8931709,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8940264,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-8968744,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-9288102,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-9585611,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-9724771,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11247895-9824350
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0017-5749
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
48
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
508-14
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:11247895-Adenomatous Polyposis Coli,
pubmed-meshheading:11247895-Adolescent,
pubmed-meshheading:11247895-Adult,
pubmed-meshheading:11247895-Child,
pubmed-meshheading:11247895-Child, Preschool,
pubmed-meshheading:11247895-Female,
pubmed-meshheading:11247895-Genes, APC,
pubmed-meshheading:11247895-Genetic Heterogeneity,
pubmed-meshheading:11247895-Genotype,
pubmed-meshheading:11247895-Germ-Line Mutation,
pubmed-meshheading:11247895-Humans,
pubmed-meshheading:11247895-Male,
pubmed-meshheading:11247895-Middle Aged,
pubmed-meshheading:11247895-Pedigree,
pubmed-meshheading:11247895-Phenotype,
pubmed-meshheading:11247895-Polymerase Chain Reaction,
pubmed-meshheading:11247895-Severity of Illness Index
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pubmed:year |
2001
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pubmed:articleTitle |
Familial adenomatous polyposis: more evidence for disease diversity and genetic heterogeneity.
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pubmed:affiliation |
Hunter Area Pathology Service, Locked Bag No 1, Hunter Regional Mail Centre, Newcastle NSW 2310, Australia. rscott@doh.health.nsw.gov.au
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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