Dysfibrinogenemia, Congenital

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

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

The major functional characteristics of fibrinogen Baltimore IV include delayed fibrin monomer polymerization which is not… Expand

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

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

 

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