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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

Robot-Assisted surgery showdown: which fix works best for rare bowel disease?

Disease control Not yet recruiting

This study compares two surgical techniques—Duhamel and Soave—for treating total colonic Hirschsprung disease, a severe birth defect where nerve cells are missing from the colon. Fifty children who had a first surgery as newborns will receive one of the two procedures. Researcher…

Phase: NA • Sponsor: Zunyi Medical College • Aim: Disease control

Last updated Jun 27, 2026 08:11 UTC