Show simple item record

dc.contributor.authorG±rses N.
dc.contributor.authorG±rses N.
dc.date.accessioned2020-06-21T09:20:39Z
dc.date.available2020-06-21T09:20:39Z
dc.date.issued1986
dc.identifier.issn0939-7248
dc.identifier.urihttps://doi.org/10.1055/s-2008-1043380
dc.identifier.urihttps://hdl.handle.net/20.500.12712/3341
dc.descriptionPubMed: 3825304en_US
dc.description.abstractA family group of 15 cases in two generations with Peutz-Jeghers syndrome has been studied and a review of the history and features of the syndrome is presented. This syndrome was detected in 10 of 15 family members in two generations. One family member underwent repeated surgery after small bowel obstruction was diagnosed. In addition, multiple polyps were removed from the rectum. Rectal bleeding dominated the clinical picture in two patients. Five of the family members had small bowel polyps, five of the siblings had polyps in the colon. Colonic polyp was also found in one patient who had a small bowel polyp. Four of the ten affected family members in two generations had mucocutaneous pigmentation. One of the siblings had died during the early postoperative period. © 1986, Georg Thieme Verlag KG Stuttgart, New York. All rights reserved.en_US
dc.language.isoengen_US
dc.relation.isversionof10.1055/s-2008-1043380en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titlePeutz-Jeghers Syndrome: A Clinical Study of a Large Family in Two Generations [Das Peutz-Jeghers-Syndrom: Klinische Studie von 2 Generationen einer gro±en Familie]en_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume41en_US
dc.identifier.issue6en_US
dc.identifier.startpage364en_US
dc.identifier.endpage368en_US
dc.relation.journalEuropean Journal of Pediatric Surgeryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record