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Erythrokeratodermia Variabilis: A Case Report

dc.contributor.authorTayan, Reyhan Uzdil
dc.contributor.authorBÜYÜKBABANİ, Nesimi
dc.contributor.authorYildirim, Gul
dc.date.accessioned2022-02-18T09:20:18Z
dc.date.available2022-02-18T09:20:18Z
dc.date.issued2007
dc.identifier.citationYildirim G., Tayan R. U. , BÜYÜKBABANİ N., "Erythrokeratodermia Variabilis: A Case Report", TURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY, cilt.41, sa.4, ss.139-141, 2007
dc.identifier.othervv_1032021
dc.identifier.otherav_32310ff1-506e-4d38-a971-12f59a0b61bd
dc.identifier.urihttp://hdl.handle.net/20.500.12627/177019
dc.description.abstractErythrokeratodermia variabilis is a rare genodermatosis inherited as an autosomal dominant trait and characterized by variable figurated erythematous patches and persistant hyperkeratotic plaques. Here we report clinical and histopathological findings of a 23 years old male patient diagnosed as erythrokeratodermia variabilis and the relevant literature is reviewed.
dc.language.isoeng
dc.subjectDermatoloji
dc.subjectDERMATOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectHealth Sciences
dc.subjectDermatology
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.titleErythrokeratodermia Variabilis: A Case Report
dc.typeMakale
dc.relation.journalTURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY
dc.contributor.departmentLepra Deri & Zuhrevi Hastaliklar Hastanesi , ,
dc.identifier.volume41
dc.identifier.issue4
dc.identifier.startpage139
dc.identifier.endpage141
dc.contributor.firstauthorID3374656


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