Mosaic epidermolytic ichthyosis - Case report

Epidermolytic ichthyosis is a rare autosomal dominant disease that manifests at birth with fragile blisters and erosions that evolve into hyperkeratotic lesions associated or not with erythroderma. When the disease is associated with a mutation in cytokeratin 1, it may be related to hyperkeratosis o...

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Detalles Bibliográficos
Autores principales: Mendes, Marcela Sena Teixeira, Kouzak, Samara Silva, Aquino, Thaissa Araújo, Takano, Gustavo Henrique Soares, Lima, Antonio de Padua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876022/
https://www.ncbi.nlm.nih.gov/pubmed/24346896
http://dx.doi.org/10.1590/abd1806-4841.20132203

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876022/
https://www.ncbi.nlm.nih.gov/pubmed/24346896
http://dx.doi.org/10.1590/abd1806-4841.20132203

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