dyschromatosis universalis hereditaria

dyschromatosis universalis hereditaria
(DUH) a rare pigmentary genodermatosis, most often seen in Japan, characterized by hyperpigmented and hypopigmented macules on the trunk, extremities, and sometimes the face that appear in infancy or early childhood. Heredity is autosomal dominant or recessive, and sporadic cases occur. There are two forms, caused by mutations at different sites: DUH1, caused by mutation at 6q24.2-q25.2, and DUH2, caused by mutation at 12q21-q23.

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