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Lupus Myelopathy in a Child

dc.contributor.authorVieira, JP
dc.contributor.authorOrtet, O
dc.contributor.authorBarata, D
dc.contributor.authorAbranches, M
dc.contributor.authorGomes, JM
dc.date.accessioned2011-04-05T10:43:46Z
dc.date.available2011-04-05T10:43:46Z
dc.date.issued2002
dc.description.abstractA 5-year-old female developed, after a 7-month period of fever, anorexia, weight loss, and a transitory cutaneous erythematous eruption, a severe acute transverse myelopathy, with a partial recovery of motor and sensory function. She had positive antinuclear and antidouble-stranded DNA antibodies but no antiphospholipid antibodies. Six months later she had massive proteinuria and restarted treatment with steroids and cyclophosphamide. Our patient is one of the youngest reported with lupus myelopathy. We discuss the clinical presentation, the magnetic resonance imaging findings, and other relevant laboratory studies of this rare but serious complication of systemic lupus erythematosus.por
dc.identifier.citationPediatr Neurol. 2002;27(4):303-306por
dc.identifier.urihttp://hdl.handle.net/10400.17/68
dc.language.isoengpor
dc.publisherElsevierpor
dc.subjectCriançapor
dc.subjectLúpus Eritematosopor
dc.subjectRessonância Magnéticapor
dc.subjectMielopatiapor
dc.subjectHDE PED
dc.subjectHDE UCI PED
dc.subjectHDE NEU PED
dc.titleLupus Myelopathy in a Childpor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage306por
oaire.citation.startPage303por
oaire.citation.titlePediatric Neurologypor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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