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
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author Kumar, Sumir
Bhoyar, Pritish
Mahajan, Bharat Bhushan
author_facet Kumar, Sumir
Bhoyar, Pritish
Mahajan, Bharat Bhushan
author_sort Kumar, Sumir
collection PubMed
description 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 adermatoglyphia in a young male with family history of the disorder.
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spelling pubmed-43757532015-03-27 A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association Kumar, Sumir Bhoyar, Pritish Mahajan, Bharat Bhushan Indian Dermatol Online J Case Report 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 adermatoglyphia in a young male with family history of the disorder. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4375753/ /pubmed/25821732 http://dx.doi.org/10.4103/2229-5178.153013 Text en Copyright: © Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kumar, Sumir
Bhoyar, Pritish
Mahajan, Bharat Bhushan
A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association
title A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association
title_full A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association
title_fullStr A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association
title_full_unstemmed A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association
title_short A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association
title_sort case of dyschromatosis universalis hereditaria with adermatoglyphia: a rare association
topic Case Report
url 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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