Publication: Erythrokeratoderma variabilis: Report of a case with rosette like lesions [Eritrokeratoderma variabilis: Rozet tipi lezyonlarla seyreden bir olgu]
| dc.contributor.authors | Kuş S., Demirçay Z., Demirkesen C. | |
| dc.date.accessioned | 2022-03-28T14:51:35Z | |
| dc.date.accessioned | 2026-01-11T06:52:21Z | |
| dc.date.available | 2022-03-28T14:51:35Z | |
| dc.date.issued | 2003 | |
| dc.description.abstract | Erythrokeratoderma variabilis (EKV) is a rare, autosomal dominantly inherited genodermatosis. The two distinct morphologic features of EKV are hyperkeratosis and transient erythema. Lesions appear during the first year of life and tend to follow a chronic course. We report a case of late onset EKV with rosette like skin lesions who responded well to the treatment with retinoids. | |
| dc.identifier.issn | 1019214X | |
| dc.identifier.uri | https://hdl.handle.net/11424/255709 | |
| dc.language.iso | tur | |
| dc.relation.ispartof | Turkderm Deri Hastaliklari ve Frengi Arsivi | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Erythrokeratoderma variabilis | |
| dc.subject | Isotretinoin | |
| dc.title | Erythrokeratoderma variabilis: Report of a case with rosette like lesions [Eritrokeratoderma variabilis: Rozet tipi lezyonlarla seyreden bir olgu] | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 208 | |
| oaire.citation.issue | 3 | |
| oaire.citation.startPage | 206 | |
| oaire.citation.title | Turkderm Deri Hastaliklari ve Frengi Arsivi | |
| oaire.citation.volume | 37 |