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pubmed-article:15482301rdf:typepubmed:Citationlld:pubmed
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pubmed-article:15482301pubmed:dateCreated2004-10-14lld:pubmed
pubmed-article:15482301pubmed:abstractTextDowling-Degos disease is a rare autosomal dominant inherited pigmentary disorder characterized by reticulate pigmentation of the flexures, prominent comedone like lesions and pitted scars. Dyschromatosis universalis hereditaria is characterized by the presence of hypopigmented as well as hyperpigmented macules. We report a family showing features of both these diseases.lld:pubmed
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pubmed-article:15482301pubmed:monthNovlld:pubmed
pubmed-article:15482301pubmed:issn0926-9959lld:pubmed
pubmed-article:15482301pubmed:authorpubmed-author:KanwarA JAJlld:pubmed
pubmed-article:15482301pubmed:authorpubmed-author:SandhuKKlld:pubmed
pubmed-article:15482301pubmed:authorpubmed-author:SaraswatAAlld:pubmed
pubmed-article:15482301pubmed:issnTypePrintlld:pubmed
pubmed-article:15482301pubmed:volume18lld:pubmed
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pubmed-article:15482301pubmed:year2004lld:pubmed
pubmed-article:15482301pubmed:articleTitleDowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family.lld:pubmed
pubmed-article:15482301pubmed:affiliationDepartment of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Sector 12, Chandigarh, 160012, India. kd_sandhu@yahoo.co.inlld:pubmed
pubmed-article:15482301pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15482301pubmed:publicationTypeCase Reportslld:pubmed