Indian Journal of Paediatric Dermatology (Jan 2017)

Sporadic dyschromatosis universalis hereditaria: A rare case report

  • Shweta Manchanda,
  • Ravish Arora,
  • M M Lingaraj

DOI
https://doi.org/10.4103/2319-7250.193025
Journal volume & issue
Vol. 18, no. 1
pp. 43 – 45

Abstract

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Dyschromatosis universalis hereditaria (DUH) is a rare genodermatoses characterized by hyperpigmented and hypopigmented macules inherited most commonly in autosomal dominant manner. We hereby report a case of DUH in an adolescent male with palmo-plantar involvement and no family history of the disorder.

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