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A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association
Dyschromatosis universalis hereditaria (DUH) is a rare, autosomal dominant genodermatosis with a peculiar reticulate pigmentary change, consisting of hyperpigmented macules mingled with hypopigmented lesions to give an overall impression of mottling. We herein report a case of DUH with adermatoglyph...
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| Publicado no: | Indian Dermatol Online J |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4375753/ https://ncbi.nlm.nih.gov/pubmed/25821732 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2229-5178.153013 |
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