Results 151 to 160 of about 695 (177)
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Segmental confetti dyschromatosis
Photodermatology, Photoimmunology & Photomedicine, 2013Mohammed I, Aljasser, Harvey, Lui
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[Dyschromatosis universalis: two cases].
Annales de dermatologie et de venereologie, 2001Universalis dyschromatosis is a rare genodermatosis. Melanogenesis dysfunction appears to be the main etiology. We report two cases, discussing the clinical features, diagnosis and etiology of this disease.A 21-year-old man was referred for a mixture of achromatic and hyperchromatic lesions that had progressed on sun-exposed skin areas since birth. The
M A, Dhaoui, N, Doss
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[Universal dyschromatosis: a familial case].
Annales de dermatologie et de venereologie, 1998Universal dyschromatosis is a generalized leucomelanodermia recognised in Japan in 1933. We report a family with universal dyschromatosis, demonstrating the mode of transmission. The ultrastructural aspects are compatible with a functional melanogenesis anomaly.A 9-year-old girl was hospitalized for recently diagnosed insulin-dependent diabetes ...
P, Schoenlaub +4 more
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Dyschromatosis universalis hereditaria: a case report
International Journal of Dermatology, 2013Shiva, Kumar +2 more
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A case of dyschromatosis universalis
Journal of the American Academy of Dermatology, 2004Latanya T. Benjamin +3 more
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Dyschromatosis universalis hereditaria (DUH)
CosmoDerma, 2022Anmol Batra, Neirita Hazarika
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