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pubmed-article:19796565pubmed:dateCreated2009-10-2lld:pubmed
pubmed-article:19796565pubmed:abstractTextJuvenile localized scleroderma (JLS) includes several subtypes including plaque morphea, linear scleroderma and the en coup de sabre type which affects face and head. The latter variety may involve the eye and the brain with various appearance and clinical complications.We describe the case of a 6-year-old boy who presented partial complex seizures, with status epilepticus, four months before the appearance of sclerodermatous skin lesions on the face. This case report raises important questions on the pathogenesis of JLS and, particularly, on the issue whether it is a mere autoimmune condition or a neuro-cutaneous disease.lld:pubmed
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pubmed-article:19796565pubmed:authorpubmed-author:MartiniGGlld:pubmed
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pubmed-article:19796565pubmed:volume27lld:pubmed
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pubmed-article:19796565pubmed:articleTitleSevere epilepsy preceding by four months the onset of scleroderma en coup de sabre.lld:pubmed
pubmed-article:19796565pubmed:affiliationDepartment of Pediatrics, University Hospital of Padova, Padova, Italy.lld:pubmed
pubmed-article:19796565pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19796565pubmed:publicationTypeCase Reportslld:pubmed