Ranging from bleeding to thrombosis, the clinical features of congenital fibrinogen
qualitative disorders, including dysfibrinogenemia and hypodysfibrinogenemia, are highly …

Introduction Congenital dysfibrinogenemia (CD) is characterized by dysfunction induced by
an abnormal fibrinogen molecule structure that results in blood coagulation dysfunction. The …

Introduction Congenital fibrinogen disorders are poorly explored in Slavic populations. The
aim of this study was to characterize the genetic background and clinical manifestations of …

Abnormal coagulation properties indicative of a dysfibrinogen were found in the plasma of a
72-year-old male with multiple myeloma (IgGĸ, stage IIIA). The patient had high paraprotein …

The clinical phenotype of patients with congenital dysfibrinogenaemia is highly
heterogeneous, from absence of symptoms to mild bleeding, or thrombosis. A few mutations …

Dysfibrinogenemia is caused by a variety of structural abnormalities in the fibrinogen
molecule, which results in a tendency for bleeding and thrombosis as well as obstetric …

Congenital dysfibrinogenemia is a rare disease characterised by inherited abnormality in
the fibrinogen molecule, resulting in functional defects. Two patients, a 26-year-old woman …

Background We reported a patient with congenital dysfibrinogenemia who was
misdiagnosed and reviewed relevant literature, in order to discuss the methods to reduce …

Three cases of congenital dysfibrinogenemia in unrelated Chi... : Medicine Three cases of
congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation …

Hereditary dysfibrinogenemia is a rare disorder wherein an inherited abnormality in
fibrinogen structure may result in defective fibrin function and/or structure. Congenital …