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Research Article Free access | 10.1172/JCI106848

Fibrinogen St. Louis: A New Inherited Fibrinogen Variant, Coincidentally Associated with Hemophilia A

Laurence A. Sherman, Lamont W. Gaston, Manuel E. Kaplan, and Alan R. Spivack

Department of Medicine, Jewish Hospital and Washington University School of Medicine, St. Louis, Missouri 63110

Department of Medicine, Veterans Administration Hospital, Minneapolis, Minnesota 55417

Find articles by Sherman, L. in: PubMed | Google Scholar

Department of Medicine, Jewish Hospital and Washington University School of Medicine, St. Louis, Missouri 63110

Department of Medicine, Veterans Administration Hospital, Minneapolis, Minnesota 55417

Find articles by Gaston, L. in: PubMed | Google Scholar

Department of Medicine, Jewish Hospital and Washington University School of Medicine, St. Louis, Missouri 63110

Department of Medicine, Veterans Administration Hospital, Minneapolis, Minnesota 55417

Find articles by Kaplan, M. in: PubMed | Google Scholar

Department of Medicine, Jewish Hospital and Washington University School of Medicine, St. Louis, Missouri 63110

Department of Medicine, Veterans Administration Hospital, Minneapolis, Minnesota 55417

Find articles by Spivack, A. in: PubMed | Google Scholar

Published March 1, 1972 - More info

Published in Volume 51, Issue 3 on March 1, 1972
J Clin Invest. 1972;51(3):590–597. https://doi.org/10.1172/JCI106848.
© 1972 The American Society for Clinical Investigation
Published March 1, 1972 - Version history
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Abstract

A patient with classical hemophilia (factor VIII deficiency) was found to have a new abnormal fibrinogen (fibrinogen St. Louis). Other family members exhibited either defect alone. Fibrinogen St. Louis was inherited as an autosomal dominant and was not associated with clinical bleeding. When compared with normal fibrinogen, fibrinogen St. Louis was found to have defective fibrin polymerization and possibly a slower release of fibrinopeptides. The prolonged thrombin times were partially corrected by calcium chloride and protamine sulfate. Ultracentrifugal sedimentation, electrophoretic mobility, DEAE chromatographic pattern, carbohydrate content, N-terminal amino acids, immunodiffusion, and immunoelectrophoretic patterns and electrophoresis of reduced and alkylated fragments were all normal. In contrast to fibrinogen St. Louis, the most similar other fibrinogen variant (fibrinogen Zurich) was found to be heterogeneous by several criteria and to have reduced hexose content.

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