Korean J Dermatol.  1994 Jun;32(3):493-497.

Dyschromatosis Universalis Hereditaria

Abstract

Dyschromatosis universalis hereditaria is a rare pigmentary disorder characterized by widespread mothed hyperpigmentation and hypopigmentation. We report a 40-year-old male patient with numerous hyperpigmenter, and hypopigmented macules all over the body except on the palms and soles. The family history revealed similar pigmentary changes in 5 other members through 4 generations, and we could guess the hereditary pattern of the disease of this family to be autosomal dominant inheritance.

Keyword

Dyschromatosis Universalis Hereditaria; Autosomal Dominant

MeSH Terms

Adult
Family Characteristics
Humans
Hyperpigmentation
Hypopigmentation
Male
Moths
Wills
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