Dyschromatosis universalis hereditaria is a type of pigmentation disorder of the skin.[1] It is characterized by dark and light spots formed like lace in a generalized distribution.[1]
Dyschromatosis universalis hereditaria | |
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Specialty | Dermatology |
Both autosomal dominant and recessive inheritance have been reported with the disorder.[2]
It has been associated with mutations in genes SASH1 and ABCB6.[citation needed]
It is a rare genodermatosis.[1]