| Literature DB >> 26312676 |
Paula Mota Medeiros1, Natália Ribeiro de Magalhães Alves1, Jeniffer Muñoz Trujillo1, Cássia Camarinha da Silva1, Paula Carolina Pessanha de Faria1, Roberto Souto da Silva1.
Abstract
Darier's disease is a rare autosomal dominant genodermatosis. It has an estimated prevalence of 1 in 55,000 to 100,000 individuals, regardless of gender. It is characterized by multiple keratotic papules on the seborrheic areas of the trunk, scalp, forehead and flexures, and the clinical picture is worsened by heat, sun exposure, perspiration and mechanical trauma. Histopathology observed loss of epithelial adhesion and abnormal keratinization. About 10% of cases present in the localized form of the disease. We report a case of segmental Darier's Disease Type I and discuss the main characteristics of this condition.Entities:
Mesh:
Year: 2015 PMID: 26312676 PMCID: PMC4540510 DOI: 10.1590/abd1806-4841.20153581
Source DB: PubMed Journal: An Bras Dermatol ISSN: 0365-0596 Impact factor: 1.896