2003
DOI: 10.1590/s0041-87812003000300005
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Antiphospholipid antibodies in 57 children and adolescents with systemic lupus erythematosus

Abstract: The frequencies of antiphospholipid antibodies in children and adolescents with lupus erythematosus were similar to those observed in adults. The positivity fluctuated during the follow-up and was not correlated with clinical and/or laboratory disease parameters.

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Cited by 8 publications
(4 citation statements)
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“…A drawback of our study is that we could test only for GM1 autoantibodies. Other autoantibodies that have been described in acute transverse myelitis include antiphospholipid antibodies, anti-Ro antibodies, and neuromyelitis optica-immunoglobulin G. [26][27][28] Neuromyelitis optica-immunoglobulin G is an aquaporin-4-specific water channel antibody, which has been associated with neuromyelitis optica and longitudinally extensive transverse myelitis in adults. 28 A recent study described the clinical and radiological features of children with neuromyelitis optica-immunoglobulin G seropositivity.…”
Section: Discussionmentioning
confidence: 99%
“…A drawback of our study is that we could test only for GM1 autoantibodies. Other autoantibodies that have been described in acute transverse myelitis include antiphospholipid antibodies, anti-Ro antibodies, and neuromyelitis optica-immunoglobulin G. [26][27][28] Neuromyelitis optica-immunoglobulin G is an aquaporin-4-specific water channel antibody, which has been associated with neuromyelitis optica and longitudinally extensive transverse myelitis in adults. 28 A recent study described the clinical and radiological features of children with neuromyelitis optica-immunoglobulin G seropositivity.…”
Section: Discussionmentioning
confidence: 99%
“…Le pic de masse osseuse est également diminué chez les enfants lupiques, ce qui soulève des problèmes de prise en charge à long terme du capital osseux avec la prise répétée de corticoïdes tout au long de la vie. L'ostéonécrose survient dans prêt de 15 % des enfants lupiques [25].…”
Section: Os Et Croissanceunclassified
“…There is predominance in females (especially in secondary APS) and no race predominance; a higher incidence was observed in young individuals and middle-aged adults, although the syndrome can manifest in children and elderly. There are reports of its occurrence in infants of less than eight months of age (6,8) .…”
Section: Introductionmentioning
confidence: 99%