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Congenital Prothrombin Deficiency

1 Jun 2009

Abstract excerpt

Prothrombin deficiency is among the rarest inherited coagulation disorders, with a prevalence of approximately 1:2,000,000. Two main phenotypes can be distinguished: (1) hypoprothrombinemia (type I deficiency), characterized by concomitantly low levels of activity and antigen; and (2) dysprothrombinemia (type II deficiency), characterized by the normal or near-normal synthesis of a dysfunctional protein. In some...

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PMID: 19598065
DOI: 10.1055/s-0029-1225759

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