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Publication:
Evaluation of Peutz-Jeghers Syndrome in a Family

dc.contributor.authorOzkan K.
dc.date.accessioned2020-06-21T09:20:40Z
dc.date.available2020-06-21T09:20:40Z
dc.date.issued1985
dc.departmentOMÜen_US
dc.department-tempOzkan, K., Department of General Surgery, Ondokuzmayis University, School of Medicine, Samsun, Turkey --en_US
dc.description.abstractFive cases of Peutz-Jeghers syndrome in one family have been studied, and a review of the history and features of the syndrome are presented. This syndrome was detected in four of six siblings and in the father. Three family members underwent surgery after small-bowel obstruction was diagnosed. A gastric polyp was removed from a fouth family member. Rectal bleeding dominated the clinical picture in two patients. Colonic polyps were also found in the three patients who had small-bowel polyps. One of the four affected siblings had mucocutaneous pigmentation, but no evidence of intestinal polyps was detected. The five affected family members have been followed up for periods of 3-1/2 to 4-1/2 years.en_US
dc.identifier.endpage213en_US
dc.identifier.issn0018-0416
dc.identifier.issue4en_US
dc.identifier.pmid4086330
dc.identifier.startpage209en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12712/3344
dc.identifier.volume33en_US
dc.language.isoenen_US
dc.relation.journalHenry Ford Hospital Medical Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleEvaluation of Peutz-Jeghers Syndrome in a Familyen_US
dc.typeArticleen_US
dspace.entity.typePublication

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