Indian Journal of Dermatology · 2015 · 13 citations · 14 references
MedicineDermatologyGeneticsDermatopathologyGenodermatosesHuman GeneticsPigmentary DisordersSyndromic GenodermatosesDermatologic DisordersPigment-related DermatosesSkin GenodermatosesSkin Pigmentation Disorders
Dyschromatosis is a pigmentary genodermatosis which presents with hyper and hypopigmented skin lesions giving a mottled appearance. It is a rare entity in India reported mainly in the East Asian population. Classically, two forms have been described; dyschromatosis universalis hereditaria (DUH) and dyschromatosis symmetrica hereditaria. Here we report four cases of DUH and one case of dyschromatosis symmetrica hereditaria from India.
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Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
Cai’e Zhang, Duanzhuo Li, Jianguo Zhang et al. · Journal of Investigative Dermatology · 2013 · 106 citations · Full text
Noriyuki Suzuki, Tamio Suzuki, Katsuhiko Inagaki et al. · Journal of Investigative Dermatology · 2005 · 92 citations
Dyschromatosis universalis hereditaria
Gomathy Sethuraman, Melba Sheila D’Souza, Devinder Mohan Thappa et al. · Clinical and Experimental Dermatology · 2002 · 41 citations
Medicine, Dermatology, Pathology +5