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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Detalles Bibliográficos
Autores principales: Kumar, Sumir, Bhoyar, Pritish, Mahajan, Bharat Bhushan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375753/
https://www.ncbi.nlm.nih.gov/pubmed/25821732
http://dx.doi.org/10.4103/2229-5178.153013

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375753/
https://www.ncbi.nlm.nih.gov/pubmed/25821732
http://dx.doi.org/10.4103/2229-5178.153013

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