Indian Dermatology Online Journal (Jan 2015)

A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association

  • Sumir Kumar,
  • Pritish Bhoyar,
  • Bharat Bhushan Mahajan

DOI
https://doi.org/10.4103/2229-5178.153013
Journal volume & issue
Vol. 6, no. 2
pp. 105 – 109

Abstract

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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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