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pubmed-article:12269736pubmed:dateCreated2002-9-24lld:pubmed
pubmed-article:12269736pubmed:abstractTextJuvenile dermatomyositis is an uncommon autoimmune disease with classic heliotrope discoloration of the eyelids, erythematous skin rash of joints, and proximal muscle weakness. It is most frequently sporadic and only rarely familial. We present juvenile dermatomyositis in a 5-year-old brother and a 3 1/2-year-old sister, both are very responsive to corticosteroids. Familial dermatomyositis can occur in different family members, and even dermatomyositis and polymyositis can coexist in the same family.lld:pubmed
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pubmed-article:12269736pubmed:authorpubmed-author:MendellJerry...lld:pubmed
pubmed-article:12269736pubmed:authorpubmed-author:TsaoChang-Yon...lld:pubmed
pubmed-article:12269736pubmed:authorpubmed-author:KisselJohn...lld:pubmed
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pubmed-article:12269736pubmed:volume17lld:pubmed
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pubmed-article:12269736pubmed:pagination540-2lld:pubmed
pubmed-article:12269736pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:12269736pubmed:year2002lld:pubmed
pubmed-article:12269736pubmed:articleTitleDermatomyositis in two siblings and a brief review of familial dermatomyositis.lld:pubmed
pubmed-article:12269736pubmed:affiliationDepartment of Pediatrics, The Ohio State University, Columbus, USA. ctsao@chi.osu.edulld:pubmed
pubmed-article:12269736pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12269736pubmed:publicationTypeCase Reportslld:pubmed