Case report: Clinicopathological characteristics of SASH1 mutation-related dyschromatosis: a rethinking of the classification of dyschromatosis [PDF]
Frontiers in GeneticsDyschromatosis, a group of pigmentary dermatoses, accompany both hyper- and hypo-pigmentation, including dyschromatosis symmetrica hereditaria (DSH), dyschromatosis universalis hereditaria (DUH), and familial progressive hyper- and hypo-pigmentation ...
Yunhua Deng
exaly +6 more sources
A Case Report of Dyschromatosis Symmetrica Hereditaria with Glucose-6-Phosphate Dehydrogenase Deficiency [PDF]
Clinical, Cosmetic and Investigational Dermatology, 2023 Panpan Wang,1 Chenyu Tang,1 Yige Zhao,1 Ping Wang2 1Department of Dermatology, Hangzhou Third People’s Hospital, Zhejiang Chinese Medical University, Hangzhou, People’s Republic of China; 2Department of Dermatology, Hangzhou Third People’s Hospital ...
Wang P, Tang C, Zhao Y, Wang P
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Acquired brachial cutaneous dyschromatosis [PDF]
JAAD Case Reports, 2023 Emily Everdell, BA +2 more
doaj +4 more sources
Dyschromatosis universalis hereditaria with keratoacanthoma: a rare presentation
Pigment International, 2022 Dyschromatosis Universalis hereditaria is a rare pigmentary disorder presenting with dyschromia of skin involving trunk and extremities arranged in mottled manner lesions, usually present in the first few years of life.
Veena
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Dyschromatosis universalis hereditaria
Indian Journal of Dermatology, 2009 Dyschromatosis universalis hereditaria is an infrequently occurring genodermatosis with a peculiar pigmentary change, consisting of varying sized hyperpigmented macules mingled with hypopigmented lesions to give an overall impression of mottling.
Naik Chandra +3 more
doaj +2 more sources
Dyschromatosis Universalis Hereditaria with Renal Failure [PDF]
Case Reports in Dermatology, 2015 Dyschromatosis universalis hereditaria (DUH) is a rare autosomal dominant inherited dermatosis which usually appears during childhood and is characterized by dyspigmentation, with both hypopigmented and hyperpigmented macules.
Salinee Rojhirunsakool +1 more
doaj +3 more sources
Dyschromatosis universalis hereditaria: a familial case with ultrastructural skin investigation
Dermatologica Sinica, 2011 Dyschromatosis universalis hereditaria (DUH) is a rare disease that is inherited both in autosomal dominant and autosomal recessive patterns. It is characterized by appearance of pinpoint to pea-sized hypo- and hyper-pigmented macules distributed in a ...
Stephen Chu-Sung Hu, Cheng-Che E Lan
exaly +3 more sources
The role of ATP-binding Cassette subfamily B member 6 in the inner ear [PDF]
Nature CommunicationsABCB6 has been implicated in dyschromatosis universalis hereditaria, a condition characterized by hyperpigmented and hypopigmented skin macules. Dyschromatosis universalis hereditaria can also present with hearing loss.
Stefanie A. Baril +19 more
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Dyschromatosis universalis hereditaria with involvement of palms
Indian Dermatology Online Journal, 2014 Dyschromatosis universalis hereditaria is a rare genodermatosis characterized by hyper- and hypopigmented macules in a reticulate pattern. Here, we present a case of DUH with involvement of the palms.
Kikkeri Narayanshetty Naveen, U S Dinesh
doaj +3 more sources
A rare presentation of dyschromatosis symmetrica hereditaria in a Canadian context: A case report [PDF]
SAGE Open Medical Case ReportsInherited reticulate pigmentary disorders (IRPD) are a group of rare dermatologic conditions characterized by distinct reticulate patterns of hyperpigmentation and/or hypopigmentation of the skin.
Sonia Czyz +2 more
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