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Sneddon's syndrome, anti-cardiolipin antibody and glomerular thrombosis.

Abstract
Sneddon's syndrome, cerebrovascular thrombosis and livedo reticularis, is often a variant of the "primary" anti-phospholipid syndrome (PAPS). We report a woman with PAPS, presenting as Sneddon's syndrome, with renal impairment and glomerular thrombosis on renal biopsy. An IgG anti-cardiolipin antibody (aCL) was identified. The aCL was purified by affinity chromatography, gel filtration chromatography and ion-exchange chromatography, assayed in a modified ELISA and found to be of the type that requires the plasma protein beta 2-GPI to bind aCL. As beta 2-GPI has anticoagulant properties it is postulated that its interaction with aCL has a pathogenic role in the thrombotic lesions associated with aCL.
AuthorsJ M Stevens, J E Hunt, A E Seymour, S A Krilis, D J Pugsley
JournalClinical nephrology (Clin Nephrol) Vol. 41 Issue 1 Pg. 18-22 (Jan 1994) ISSN: 0301-0430 [Print] Germany
PMID8137565 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Antibodies, Anticardiolipin
  • Immunoglobulin G
Topics
  • Adult
  • Antibodies, Anticardiolipin (analysis)
  • Antiphospholipid Syndrome (complications, immunology, pathology)
  • Female
  • Humans
  • Immunoglobulin G (analysis)
  • Intracranial Embolism and Thrombosis (etiology, immunology, pathology)
  • Kidney Diseases (etiology)
  • Kidney Glomerulus
  • Pigmentation Disorders (etiology)
  • Skin Diseases, Vascular (etiology, immunology, pathology)
  • Syndrome
  • Thrombosis (etiology)

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