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Rare coagulation disorders: fibrinogen, factor VII and factor XIII
Author(s) -
Moerloose P.,
Schved J.F.,
Nugent D.
Publication year - 2016
Publication title -
haemophilia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.213
H-Index - 92
eISSN - 1365-2516
pISSN - 1351-8216
DOI - 10.1111/hae.12965
Subject(s) - fibrinogen , medicine , coagulation disorder , coagulation , factor xiii , factor vii , immunology
Rare coagulation disorders ( RCD s) 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 ( VKCFD s). 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 .