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Title of Journal: Pediatr Nephrol

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Abbravation: Pediatric Nephrology

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Springer-Verlag

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DOI

10.1002/jso.20728

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1432-198X

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Catastrophic antiphospholipid antibody syndrome

Authors: Jyoti Sharma Srilekha Karthik Subba Rao Kishore Phadke Julian Crasta Isha Garg
Publish Date: 2005/04/26
Volume: 20, Issue: 7, Pages: 998-999
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Abstract

Antiphospholipid antibody syndrome APS is characterized by recurrent thrombosis with the presence of circulating antiphospholipid antibodies A diagnosis of APS requires the presence of at least one clinical and one laboratory criteria detection of aCL IgG or IgM antibodies or the presence of lupus anticoagulant on two or more consecutive occasions 6 weeks apart A severe rapidly progressive form characterized by clinical involvement of at least three different organ systems with histopathological evidence of small and large vessel occlusion is termed catastrophic antiphospholipid syndrome Early recognition of APS is crucial since aggressive management can result in a favorable outcome We present the case of a 12yearold boy who presented with a devastating illness with multiple thrombotic episodes and rapidly progressive renal failure

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  6. Vincristine treatment in steroid-dependent nephrotic syndrome
  7. Roles of renal ammonia metabolism other than in acid–base homeostasis
  8. Congenital nephrotic syndrome with prolonged renal survival without renal replacement therapy
  9. Rhabdomyolysis: pathogenesis of renal injury and management
  10. Long-term outcome of children treated with rituximab for idiopathic nephrotic syndrome
  11. The clinical and laboratory features of Chinese Han anti-factor H autoantibody-associated hemolytic uremic syndrome
  12. Erratum to: Health-related quality of life and mental health in parents of children with hemolytic uremic syndrome
  13. Erratum to: Health-related quality of life and mental health in parents of children with hemolytic uremic syndrome
  14. Success of eculizumab in the treatment of atypical hemolytic uremic syndrome
  15. Fungal peritonitis in children on peritoneal dialysis
  16. A case of dense deposit disease associated with a group A streptococcal infection without the involvement of C3NeF or complement factor H deficiency
  17. Intravenous delivery of cysteamine for the treatment of cystinosis: association with hepatotoxicity
  18. An unusual cause of pleural effusion, urinothorax in a child with urinary stone disease
  19. Genetic polymorphisms and risk for acute renal failure in preterm neonates
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  22. International validation of a urinary biomarker panel for identification of active lupus nephritis in children
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  26. Nutritional management and growth in children with chronic kidney disease
  27. Hypertension and hemodialysis: pathophysiology and outcomes in adult and pediatric populations
  28. Age-related differences in Adriamycin-induced nephropathy
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  31. Re-establishment of the ERA-EDTA Registry
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