Dysfibrinogenemia, Congenital

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

Congenital dysfibrinogenemia is a qualitative congenital fibrinogen disorder characterized by normal antigen levels of a… (More)

Dysfibrinogenemia is an autosomally dominant disorder that can result in excessive bleeding as well as specific pregnancy… (More)

BACKGROUND Congenital dysfibrinogenemia is a functional disorder of the fibrinogen that represents a rare cause of thrombophilia… (More)

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

A 34-yr-old male commercial pilot developed a painful swollen right upper arm following an episode of trauma. Venography… (More)

OBJECTIVES To review the state of the art relating to congenital dysfibrinogenemia as a potential risk factor for thrombosis, as… (More)

Congenital dysfibrinogenemia is a rare cause of unexplained thrombosis. However, most individuals with dysfibrinogenemia are… (More)

Congenital dysfibrinogenemia is based on different alterations in the structure of the fibrinogen molecule leading to a variety… (More)

Congenital dysfibrinogenemia was found in a patient with venous thrombosis. Blood clot lysis was prolonged and suggested an… (More)