Publication:
Erythrokeratoderma variabilis: Report of a case with rosette like lesions [Eritrokeratoderma variabilis: Rozet tipi lezyonlarla seyreden bir olgu]

Loading...
Thumbnail Image

Date

Authors

Journal Title

Journal ISSN

Volume Title

Publisher

Research Projects

Organizational Units

Journal Issue

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.

Description

Citation

Endorsement

Review

Supplemented By

Referenced By