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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
8
|
| pubmed:dateCreated |
1998-9-3
|
| pubmed:abstractText |
Choledochal cysts and familial adenomatous polyposis are infrequent disorders that are often manifest in childhood or in early adult life. The rarity and early presentation of these diseases suggests a genetic basis, which has been established for familial polyposis but not for choledochal cysts. We report a case of a 26-yr-old woman with both disorders and offer an alternative genetics-based etiology for the formation of choledochal cysts.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Aug
|
| pubmed:issn |
0002-9270
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
93
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
1377-9
|
| pubmed:dateRevised |
2005-11-16
|
| pubmed:meshHeading |
pubmed-meshheading:9707074-Adenomatous Polyposis Coli,
pubmed-meshheading:9707074-Adult,
pubmed-meshheading:9707074-Anastomosis, Roux-en-Y,
pubmed-meshheading:9707074-Choledochal Cyst,
pubmed-meshheading:9707074-Female,
pubmed-meshheading:9707074-Humans,
pubmed-meshheading:9707074-Jejunostomy,
pubmed-meshheading:9707074-Pancreatitis,
pubmed-meshheading:9707074-Recurrence,
pubmed-meshheading:9707074-Reoperation
|
| pubmed:year |
1998
|
| pubmed:articleTitle |
Type I choledochal cyst in association with familial adenomatous polyposis.
|
| pubmed:affiliation |
Department of Surgery, University of North Carolina, Chapel Hill 27599-7210, USA.
|
| pubmed:publicationType |
Journal Article,
Review,
Case Reports
|