Congenital fibrinogen deficiency

Congenital deficiencies of fibrinogen are coagulation disorders characterized by bleeding symptoms ranging from mild to severe resulting from reduced quantity and/or quality of circulating fibrinogen. Afibrinogenemia (complete absence of fibrinogen) and hypofibrinogenemia (reduced plasma fibrinogen concentration) correspond to quantitative anomalies of fibrinogen while dysfibrinogenemia corresponds to a functional anomaly of fibrinogen. Hypo- and dysfibrinogenemia may be frequently combined (hypodysfibrinogenemia).

Also known as: congenital fibrinogen deficiency, fibrinogen deficiency, congenital

16 clinical trials for this condition and its sub-types, 2 tagged with Congenital fibrinogen deficiency itself.