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Dyschromatosis universalis hereditaria

MONDO:0000736

A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution.

Also known as: dyschromatosis universalis, DUH

2 clinical trials for this condition and its sub-types.

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Sub-types

Dyschromatosis universalis hereditaria 1 (0) Dyschromatosis universalis hereditaria 2 (0) Dyschromatosis universalis hereditaria 3 (0)

Broader categories

Disease (680) Hereditary disease (176) Skin disorder (132) Hyperpigmentation of the skin (15) Human disease (14) Skin pigmentation disorder (11) Hereditary skin disorder (6) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)

Not yet recruiting 1 Completed 1

New serums take on hydroquinone in skin brightening showdown

Symptom relief Completed

This 4-week pilot study tested two brightening serums against 4% hydroquinone in 18 adults with hyperpigmentation or melasma. Each participant used different products on each side of their face to compare results. The goal was to see if the serums could improve skin tone evenness…

Phase: NA • Sponsor: Revision Skincare • Aim: Symptom relief

Last updated Jun 27, 2026 13:06 UTC