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A rare multisystem disorder: dyskeratosis congenita with gastric carcinoma

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dc.contributor.authorGürel, Selim
dc.contributor.buuauthorGÜREL, SELİM
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentGastroenteroloji Ana Bilim Dalı
dc.contributor.scopusid7003706434
dc.date.accessioned2025-08-07T07:16:22Z
dc.date.issued1999-12-01
dc.description.abstractWe report a rare case of dyskeratosis congenita with gastric carcinoma in an adult man whose brother had the same disease. Dyskeratosis congenita is an inherited X-linked disorder characterized by nail dystrophy, skin pigmentation, mucosal leukoplakia and increased incidence of malignancy. Squamous skin carcinoma is also often seen in this disorder. Dyskeratosis in conjuction with gastric carcinoma is very infrequently reported in the literature.
dc.identifier.endpage43
dc.identifier.issn1128-935X
dc.identifier.issue1
dc.identifier.scopus2-s2.0-0032697157
dc.identifier.startpage41
dc.identifier.urihttps://hdl.handle.net/11452/54410
dc.identifier.volume27
dc.indexed.scopusScopus
dc.language.isoen
dc.relation.journalInternational Journal of Medicine Biology and the Environment
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectGastric cancer
dc.subjectDyskeratosis congenita
dc.subject.scopusDyskeratosis Congenita and Telomere Biology Insights
dc.titleA rare multisystem disorder: dyskeratosis congenita with gastric carcinoma
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Gastroenteroloji Ana Bilim Dalı
local.indexed.atScopus
relation.isAuthorOfPublicationd7a9ea11-69fc-4122-a365-8fb2123512e6
relation.isAuthorOfPublication.latestForDiscoveryd7a9ea11-69fc-4122-a365-8fb2123512e6

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