Xerodermapigmentosum and nursing care

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dc.contributor.authorGöz F.
dc.contributor.authorErkan M.
dc.contributor.authorSaldus B.
dc.date.accessioned2024-04-24T18:43:37Z
dc.date.available2024-04-24T18:43:37Z
dc.date.issued2007
dc.departmentDicle Üniversitesien_US
dc.description.abstractXeroderma pigmentosum (XP) is a rare hereditary disorder. It is characterized by enzymatic defects in the repair of ultraviolet-induced DNA damage, hypersensitivity of the skin to sunlight, photosensitivity, persistent erythema and hyperpigmentation. Cutaneous damage caused by ultraviolet radiation predisposes to cutaneous malignancies. This disease began at the age of 1 in our 4-year-old male patient. Our patient's clinical findings and prognosis fit the description in the literature. The nursing interventions for this case are explained.en_US
dc.identifier.endpage90en_US
dc.identifier.issn1016-5134
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-34250785779en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage89en_US
dc.identifier.urihttps://hdl.handle.net/11468/24226
dc.identifier.volume19en_US
dc.indekslendigikaynakScopus
dc.language.isotren_US
dc.relation.ispartofSENDROMen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleXerodermapigmentosum and nursing careen_US
dc.title.alternativeKseroderma pigmentosum ve hemşirelik bakimien_US
dc.typeArticleen_US

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