Dyschromatosis universalis hereditaria
Medical condition
From Wikipedia, the free encyclopedia
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 | |
|---|---|
| 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]