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      Rare coagulation disorders: fibrinogen, factor VII and factor XIII.

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          Abstract

          Rare coagulation disorders (RCDs) include the inherited deficiencies of fibrinogen, factor (F) II, FV, combined FV and VIII, FVII, FX, combined FVII and X, FXI, FXIII and combined congenital deficiency of vitamin K-dependent factors (VKCFDs). Despite their rarity, a deep comprehension of all these disorders is essential to really understand haemostasis. Indeed, even if they share some common features each RCD has some particularity which makes it unique. In this review, we focus on three disorders: fibrinogen, FVII and FXIII.

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          Author and article information

          Journal
          Haemophilia
          Haemophilia : the official journal of the World Federation of Hemophilia
          Wiley-Blackwell
          1365-2516
          1351-8216
          Jul 2016
          : 22 Suppl 5
          Affiliations
          [1 ] Division of Angiology and Haemostasis, University Hospitals and Faculty of Medicine, Geneva, Switzerland.
          [2 ] Hemophilia treatment Center, Montpellier, France.
          [3 ] Department of Hematology, Children's Hospital of Orange County, Orange, CA, USA.
          Article
          10.1111/hae.12965
          27405678
          79d58eaf-d9f1-4335-b5d2-bf164459ebcd
          History

          fibrinogen,factor VII,factor XIII,bleeding
          fibrinogen, factor VII, factor XIII, bleeding

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