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A functional abnormal antithrombin III (AT III) deficiency: AT III Charleville.

Abstract
An antithrombin III (AT III) functional defect (AT III Charleville) was discovered in a patient presenting with recurrent venous thrombosis. Both anti-activated factor X (anti Xa) and antithrombin activity were decreased, in the absence and in the presence of heparin, while protein concentration was normal in an immunological assay. The abnormal AT III copurified with functional AT III using insolubilized heparin affinity chromatography. Polyacrylamide gel electrophoresis (PAGE) and high pressure liquid chromatography (HPLC) on a TSK column suggest that AT III Charleville forms unstable complexes with thrombin from which a modified protein is rapidly released.
AuthorsM Aiach, M Nora, J N Fiessinger, M Roncato, D François, M A Gelas
JournalThrombosis research (Thromb Res) Vol. 39 Issue 5 Pg. 559-70 (Sep 01 1985) ISSN: 0049-3848 [Print] United States
PMID4082101 (Publication Type: Case Reports, Journal Article)
Chemical References
  • antithrombin III Charleville
  • Antithrombin III
  • Heparin
  • Thrombin
Topics
  • Adult
  • Antithrombin III (genetics, isolation & purification)
  • Antithrombin III Deficiency
  • Female
  • Heparin (pharmacology)
  • Humans
  • Immunoelectrophoresis, Two-Dimensional
  • Male
  • Pedigree
  • Thrombin (metabolism)
  • Thrombophlebitis (blood, genetics)

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