Oculoectodermal syndrome: twentieth described case with new manifestations

Oculoectodermal syndrome is a rare disease characterized by the association of aplasia cutis congenita, epibulbar dermoids, and other abnormalities. This report describes the twentieth case of the disease. We report a 4-year-old female child who presented with the classical features of the syndrome:...

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Detalles Bibliográficos
Autores principales: Figueiras, Daniela de Almeida, Leal, Deborah Maria de Castro Barbosa, Kozmhinsky, Valter, Querino, Marina Coutinho Domingues, Regueira, Marina Genesia da Silva, Studart, Maria Gabriela de Morais
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325028/
https://www.ncbi.nlm.nih.gov/pubmed/28300929
http://dx.doi.org/10.1590/abd1806-4841.20164409

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325028/
https://www.ncbi.nlm.nih.gov/pubmed/28300929
http://dx.doi.org/10.1590/abd1806-4841.20164409

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