Publication:
Dyschromatosis Universalis Hereditaria

creativeworkseries.issn1812-2027
dc.contributor.authorBista, M
dc.contributor.authorAgrawal, S
dc.contributor.authorAgrawal, Y
dc.date.accessioned2025-12-11T07:30:51Z
dc.date.available2025-12-11T07:30:51Z
dc.date.issued2021
dc.descriptionBista M,1 Agrawal S,1 Agrawal Y2 1Department of Dermatology and Venerology 2Department of Pathology B.P. Koirala Institute of Health Sciences, Dharan, Nepal
dc.description.abstractABSTRACT Dyschromatosis universalis hereditaria (DUH) is a rare pigmentary genodermatosis usually inherited in autosomal dominant fashion characterized by multiple pinpoint to pea-sized hypo- and hyper-pigmented macules arranged in reticulate pattern that develops within the first few years of life. An 11 years old boy presented with multiple gradually progressive asymptomatic hypopigmented macules on hyperpigmented background on trunk, extremities and face since 2 years of age. Family history was absent. Punch biopsies revealed increased number of melanocytes in the epidermis with basal cell vacuolar alteration and pigmentary incontinence and perivascular infiltration by lymphocytes and melanophages in the dermis. We herein present a sporadic case of dyschromatosis universalis hereditaria. KEY WORDS Dyschromatosis universalis hereditaria, Reticulate pigmentation
dc.identifier.urihttps://hdl.handle.net/20.500.14572/3545
dc.language.isoen_US
dc.publisherKathmandu University
dc.subjectDyschromatosis universalis hereditaria
dc.subjectReticulate pigmentation
dc.titleDyschromatosis Universalis Hereditaria
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage147
oaire.citation.startPage146
relation.isJournalIssueOfPublicationdd71608f-309e-4987-a5c2-264b37b74bcb
relation.isJournalIssueOfPublication.latestForDiscoverydd71608f-309e-4987-a5c2-264b37b74bcb
relation.isJournalOfPublicationa782b7ff-cf89-4178-ad1c-11ed89cfe1bd

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