Photoletter to the editor: Dyschromatosis universalis hereditaria: an infrequently occurring entity in Europe

Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis mainly described in asian subjects. Here, we report a case of a caucasian 11-year-old boy with DUH and an unaffected twin brother. Parents were not consanguineous. A review of the main phenotical, clinical and hystological aspects...

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Bibliografiske detaljer
Main Authors: Merino de Paz, Nayra, Rodríguez-Martin, Marina, Contreras Ferrer, Patricia, Pestana-Eliche, Maria, Martin-Herrera, Antonio, Noda-Cabrera, Antonio
Format: Artigo
Sprog:Inglês
Udgivet: Specjalisci Dermatolodzy 2012
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3470799/
https://ncbi.nlm.nih.gov/pubmed/23091589
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3315/jdcr.2012.1112
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