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dc.contributor.authorEvans, Sibel Ersoy
dc.date.accessioned2019-12-10T10:52:33Z
dc.date.available2019-12-10T10:52:33Z
dc.date.issued2013
dc.identifier.issn1019-214X
dc.identifier.urihttps://doi.org/10.4274/turkderm.47.s18
dc.identifier.urihttp://hdl.handle.net/11655/14556
dc.description.abstractThe cutaneous features of some genetic diseases that manifest during childhood might be the first signs of predisposition to cancer; therefore, early recognition of such clinical findings as well as necessary follow-up are vital. This review focuses in particular on nevoid basal cell carcinoma, Cowden syndrome, neurofibromatosis type 1, tuberous sclerosis, Peutz-Jegher's syndrome, dyskeratosis congenita, and xeroderma pigmentosum. These genodermatoses, are characterised by predisposition to skin cancer or cancer in other organs; as such this review aimed to highlight their diagnostic clinical features.
dc.language.isotur
dc.publisherTurkish Soc Dermatology Venerology
dc.relation.isversionof10.4274/turkderm.47.s18
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectDermatology
dc.titleMalignite ile İlişkili Genodermatozlar
dc.title.alternativeMalignancy Associated Genodermatoses
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalTurkderm-Archives Of The Turkish Dermatology And Venerology
dc.contributor.departmentDeri ve Zührevi Hastalıkları
dc.identifier.volume47
dc.identifier.startpage103
dc.identifier.endpage110
dc.description.indexWoS
dc.description.indexScopus


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