Results 61 to 70 of about 4,456 (153)
Background The usefulness of the activated partial thromboplastin time (APTT) waveform has been reported in hemophilia, acquired hemophilia and monitoring for anticoagulants.
Kei Suzuki +8 more
doaj +1 more source
A case of hypofibrinogenemia presenting with submental hamatoma
Hereditary hypofibrinogenemia is a rare disease and the usual presentation is difficult to stop bleeding or hamatoma in the muscle or intracranial space after injury. There may also be adverse pregnancy outcome, and increased tendency to thromÂbosis. The
Mujahida Rahman +2 more
doaj +1 more source
Congenital hypofibrinogenemia.
Congenital afibrinogenemia/hypofibrinogenemia is an extremely rare coagulation disorder. We describe a case of congenital hypofibrinogenemia in a 6-year female child, who presented with recurrent ecchymotic spots with no frank bleeding.
Neeraj, Awasthy +3 more
openaire +1 more source
Tigecycline-associated hypofibrinogenemia: A case report and review of the literature
Tigecycline, a glycylcycline-derived antibacterial that has been approved for the treatment of various infections, is widely used for multi-drug resistant bacteria.
Pei-Chun Wu, Chien-Chih Wu
doaj +1 more source
Acute Promyelocytic Leukemia Associated with Hypofibrinogenemia [PDF]
Abstract This study of 17 cases further establishes acute promyelocytic leukemia with hypofibrinogenemia as a distinct entity. This disease has a rapid course characterized by severe hemorrhagic manifestations and a poor response to therapy.
openaire +2 more sources
Background: inherited fibrinogen disorders are characterized by a spectrum of quantitative or qualitative fibrinogen deficiency associated with both a hemorrhagic and thrombotic risk.
Renato Marino +9 more
doaj +1 more source
Chiari I Malformation and Intramedullary Hemorrhage in a Female Patient with Klippel Trenaunay Syndrome: A Rare Case Report Study [PDF]
Chiari I Malformation and Intramedullary Hemorrhage in a Female Patient with Klippel Trenaunay Syndrome: A Rare Case Report ...
Kalliopi Magounaki +5 more
doaj
A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family
Congenital fibrinogen disorders are a group of coagulation deficiencies caused by fibrinogen defects and are divided into four types, including afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia, and hypodysfibrinogenemia. In this study, we collected
Xiaoying Xie +5 more
doaj +1 more source
Introduction: Pit viper envenomation may cause coagulopathy. The coagulopathy has been treated with crotalidae polyvalent immune fragment antigen-binding (Fab) ovine antivenom for the last few decades in the United States and usually corrects the acute ...
Jean C.Y. Lo, E. Lea Walters, Brian Wolk
doaj +1 more source
Urticaria, Fever, and Hypofibrinogenemia [PDF]
Verena, Mohr +5 more
openaire +2 more sources

