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Sporadic dyschromatosis universalis hereditaria: A rare case report

 Department of Dermatology, Venereology and Leprology, J.J.M. Medical College, Davangere, Karnataka, India

Correspondence Address:
Shweta Manchanda,
Room No. 9, Bapuji Hospital, J.J.M. Medical College, Davangere, Karnataka
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/2319-7250.193025

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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