Open AccessA case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association
Author(s) -
Sumir Kumar,
Pritish A Bhoyar,
Bharat Bhushan Mahajan
Publication year - 2015
Publication title -
indian dermatology online journal
Language(s) - English
Resource type - Journals
eISSN - 2249-5673
pISSN - 2229-5178
DOI - 10.4103/2229-5178.153013
Subject(s) - genodermatosis , medicine , dermatology , genetics , biology , gene
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.