1954Acta PaediatricaRequires access

Congenital Idiopathic Hypoprothrombinemia1

S. Van Creveld

Open publisher page 19 citations

Abstract

Summary Attention is drawn to the fact that a prolongation of the prothrombin time existing from birth may be due to a decrease of prothrombin, to a decrease of the recently described prothrombin conversion factors, and to a combination of both. Therefore, apart from true hypoprothrombinemia, pseudo‐hypo‐prothrombinemia must be distinguished. These advances in our knowledge make it necessary to reconsider cases earlier indicated as congenital idiopathic hypoprothrombinemia. A family with true congenital idiopathic, hypoprothrombinemia is described in detail. With the plasma of one of the members of this family the problem of the formation of thromboplastin was studied.

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What this paper is about

Summary Attention is drawn to the fact that a prolongation of the prothrombin time existing from birth may be due to a decrease of prothrombin, to a decrease of the recently described prothrombin conversion factors, and to a combination of both. Therefore, apart from true hypoprothrombinemia, pseudo‐hypo‐prothrombinemia must be distinguished. These advances in our knowledge make it necessary to reconsider cases earlier indicated as congenital idiopathic hypoprothrombinemia. A family with true congenital idiopathic, hypoprothrombinemia is described in detail. With the plasma of one of the members of this family the problem of the formation of thromboplastin was studied.

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OpenAlex reports 19 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Summary Attention is drawn to the fact that a prolongation of the prothrombin time existing from birth may be due to a decrease of prothrombin, to a decrease of the recently described prothrombin conversion factors, and to a combination of both. Therefore, apart from true hypoprothrombinemia, pseudo‐hypo‐prothrombinemia must be distinguished. These advances in our knowledge make it necessary to reconsider cases earlier indicated as congenital idiopathic hypoprothrombinemia. A family with true congenital idiopathic, hypoprothrombinemia is described in detail. With the plasma of one of the members of this family the problem of the formation of thromboplastin was studied.

Key concepts: Hypoprothrombinemia, Medicine, Thromboplastin, PROTHROMBIN COMPLEX, Prothrombin time, Pediatrics, Partial thromboplastin time, Coagulation

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