Dysfibrinogenemia, Congenital

AbstractCongenital dysfibrinogenemia (CD) is a qualitative fibrinogen disorder caused by an abnormal fibrinogen molecule… Expand

We conducted a multicenter study of 101 patients with congenital dysfibrinogenemia (CD) to characterize the incidence of… Expand

INTRODUCTION Congenital dysfibrinogenemia (CD) is a rare qualitative disorder of fibrinogen (Fg) with heterogeneous clinical… Expand

Congenital dysfibrinogenemia is a rare disease characterised by inherited abnormality in the fibrinogen molecule, resulting in… Expand

INTRODUCTION Various dysfibrinogenemias have been described worldwide. This paper describes two new cases of dysfibrinogenemia… Expand

Two young siblings (a male of 21 and his sister of 26 years) suffered from arterial thrombosis episodes of the carotid and… Expand

Congenital severe dysfibrinogenemia was discovered in a small Saudi family. Their single child exhibited abnormal severe bleeding… Expand

A new case of congenital dysfibrinogenemia, in which the patient has severe thrombotic disease, is reported. The abnormal… Expand

 

A dysfibrinogenemia (fibrinogen Bethesda) was detected in a 9 yr old male of Mexican-English extraction who had a lifelong… Expand