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Updated: Mar 18, 2026

Measurement of Factor V Activity in Human Plasma Using a Microplate Coagulation Assay
Published on: September 9, 2012
Rare coagulation disorders: fibrinogen, factor VII and factor XIII
P de Moerloose1, J-F Schved2, D Nugent3
1Division of Angiology and Haemostasis, University Hospitals and Faculty of Medicine, Geneva, Switzerland.
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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