Dyschromatosis universalis hereditaria 3
MONDO:0014169Any dyschromatosis universalis hereditaria in which the cause of the disease is a mutation in the ABCB6 gene.
Also known as: ABCB6 dyschromatosis universalis hereditaria, dyschromatosis universalis hereditaria 3, dyschromatosis universalis hereditaria caused by mutation in ABCB6, dyschromatosis universalis hereditaria type 3, DUH3
8 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
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New serums take on hydroquinone in skin brightening showdown
Symptom relief CompletedThis 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
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AI could cut skin specialist wait times, study hints
Knowledge-focused CompletedThis study tested an artificial intelligence algorithm designed to help primary care doctors decide whether a patient with a skin condition really needs to see a dermatologist. Researchers enrolled 200 adults with skin problems and had their doctors take photos of the affected ar…
Sponsor: AI Labs Group S.L • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:11 UTC