Results 101 to 110 of about 1,069 (160)
Congenital hypofibrinogenemia with bone cyst: a case report with review of literature
Congenital hypofibrinogenemia is a rare autosomal recessive condition leading to low plasma fibrinogen levels, affecting approximately one in a million.
Yelugoti, V, Mamadapur, M
core
Management of Young and Ageing Women with Afibrinogenemia and Hypofibrinogenemia
Congenital afibrinogenemia and hypofibrinogenemia are rare hereditary coagulation disorders characterized by the absence or deficiency of fibrinogen.
De Moerloose, Philippe +1 more
core +1 more source
, 2008 Congenital hypofibrinogenemia is a rare bleeding disorder characterized by abnormally low levels of fibrinogen in plasma, generally due to heterozygous mutations in one of the three fibrinogen genes (FGA, FGB, and FGG, coding for Aalpha, Bbeta, and gamma
M.L. Tenchini +7 more
core +1 more source
Thoracic aortic surgery often causes massive bleeding due to coagulopathy. Hypofibrinogenemia is one of the major causative factors, but the utility of the intraoperative administration of fibrinogen concentrate has not yet been proven.
OSHIMA, HIDEKI +9 more
core
A Lesser Known Side Effect of Tigecycline: Hypofibrinogenemia
Turkish Journal of Hematology, 2018 Fulya Yılmaz Duran +2 more
doaj +1 more source
A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family
HereditasCongenital 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
Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain gene
Haematologica, 2006 BACKGROUND AND OBJECTIVES: Afibrinogenemia and hypofibrinogenemia are rare inherited coagulation disorders characterized by hemorrhagic manifestations of variable entity and by plasma fibrinogen deficiency.
L Monaldini +6 more
doaj
Intraosseous pseudotumor in a child with hypofibrinogenemia
Pediatric Radiology, 2014 Intraosseous pseudotumor (i.e. chronic, encapsulated, hemorrhagic fluid collection that can be seen in any portion of the tubular bones) is an uncommon complication of severe hemophilia; however, it can occur with other rare bleeding disorders. We present the case of an 11-year-old girl with hypofibrinogenemia who had multiple intramedullary lesions ...
AYDINGÖZ, ÜSTÜN +2 more
openaire +4 more sources