Literature DB >> 18698184

Antiphospholipid syndrome in children.

Tadej Avcin1.   

Abstract

PURPOSE OF REVIEW: Antiphospholipid syndrome is considered as the most common acquired hypercoagulation state of autoimmune disorder in children. Besides vascular occlusion, antiphospholipid antibodies have been associated with various nonthrombotic clinical manifestations. This review highlights recent clinical advances in the field of neonatal and pediatric antiphospholipid syndrome and emphasizes differences in relation to the antiphospholipid syndrome in adult population. RECENT
FINDINGS: Neonatal antiphospholipid syndrome is a rare clinical entity characterized by neonatal thrombotic disease due to the transplacental passage of maternal antiphospholipid antibodies. There is growing evidence that transplacentally transferred antiphospholipid antibodies act as a risk factor, but are not usually a sufficient condition for thrombosis and other thrombophilic risk factors should be systematically evaluated. Long-term studies of children born to antiphospholipid-antibody-positive mothers provided the evidence of possible neurodevelopmental changes in these children and regular neuropsychological assessments are recommended. Data from the pediatric antiphospholipid syndrome studies have confirmed that antiphospholipid-antibody-related thromboses in children are frequently associated with multiple antiphospholipid antibodies positivity and concomitant presence of inherited prothrombotic disorders. Children with antiphospholipid syndrome have frequently demonstrated associated nonthrombotic manifestations, particularly hematological, skin and neurological manifestations. Comparisons between children with primary antiphospholipid syndrome and antiphospholipid syndrome associated with autoimmune disease have recognized certain differences that suggest two distinct subgroups with specific clinical characteristics.
SUMMARY: Clinical and laboratory characterization of pediatric patients with antiphospholipid syndrome continues to improve and implies some important differences between antiphospholipid syndrome in pediatric and adult populations.

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Year:  2008        PMID: 18698184     DOI: 10.1097/BOR.0b013e3283060a8c

Source DB:  PubMed          Journal:  Curr Opin Rheumatol        ISSN: 1040-8711            Impact factor:   5.006


  4 in total

1.  Acute adrenal failure as the presenting feature of primary antiphospholipid syndrome in a child.

Authors:  Nicola Improda; Maria Alessio; Donatella Capalbo; Giustina Russo; Ida D'Acunzo; Loredana Palamaro; Claudio Pignata; Mariacarolina Salerno
Journal:  Ital J Pediatr       Date:  2012-09-20       Impact factor: 2.638

2.  The Pathogenicity of Anti-β2GP1-IgG Autoantibodies Depends on Fc Glycosylation.

Authors:  Christoph Fickentscher; Iryna Magorivska; Christina Janko; Mona Biermann; Rostyslav Bilyy; Cecilia Nalli; Angela Tincani; Veronica Medeghini; Antonella Meini; Falk Nimmerjahn; Georg Schett; Luis E Muñoz; Laura Andreoli; Martin Herrmann
Journal:  J Immunol Res       Date:  2015-06-22       Impact factor: 4.818

3.  Antiphospholipid Syndrome: Multiple Manifestations in a Single Patient-A High Suspicion Is Still Needed.

Authors:  Uroosa Ibrahim; Shiksha Kedia; Gwenalyn Garcia; Jean Paul Atallah
Journal:  Case Rep Med       Date:  2017-05-23

4.  Recurrent arterial and venous thrombosis in a 16-year-old boy in the course of primary antiphospholipid syndrome despite treatment with low-molecular-weight heparin: a case report.

Authors:  Malgorzata Biernacka-Zielinska; Joanna Lipinska; Joanna Szymanska-Kaluza; Jerzy Stanczyk; Elzbieta Smolewska
Journal:  J Med Case Rep       Date:  2013-08-23
  4 in total

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