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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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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Specjalisci Dermatolodzy
2012
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| Matèries: | |
| Accés en línia: | 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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