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Fibrinogen and dysfibrinogenemia.
Annals of clinical and laboratory science, 1981The fibrinogen molecule is becoming increasingly understood. Amino acid sequencing has been undertaken and studies of abnormal fibrinogens are leading to a more functional concept of its structure. Acquired dysfibrinogenemia appears to be a more common problem than previously thought, and may be found in patients with liver disease, cancer ...
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Congenital (hypo-)dysfibrinogenemia and bleeding: A systematic literature review
Thrombosis Research, 2022Qiulan Ding
exaly
[Obstetrical management in dysfibrinogenemia].
Geburtshilfe und Frauenheilkunde, 1990Dysfibrinogenaemia is an inherited disorder, characterised by a plasmafibrinogen in normal concentration, but of abnormal quality due to impaired release of fibrinopeptides and/or impaired aggregation of fibrinomonomers. The typical abnormalities of the laboratory findings will be demonstrated by presenting the case reports of 4 patients with 5 ...
H, Heidegger, M, Spannagel, W, Schramm
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Dysfibrinogenemia as Thrombophilic Factor
1992The prevalence of congenital disfibrinogenemia in venous thrombosis is approximately 0.5% as deduced from 5 studies on familial thrombophilia including a total of 1871 patients [1-5]. This is low in comparison with the prevalence of deficiencies of anticoagulation factors such as antithrombin III protein S and protein C, which together account for one ...
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Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region
Hematology, 2021Liqun Xiang +2 more
exaly