The dysfibrinogenemias consist of three types of fibrinogen disorders in which a critical blood clotting factor, fibrinogen, circulates at normal levels...
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Fibrinogen (section Congenital dysfibrinogenemia)
congenital dysfibrinogenemia. Fibrinogen Aα-Chain amyloidosis has not associated with abnormal bleeding or thrombosis. Acquired dysfibrinogenemia is a rare...
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distinct fibrinogen disorders: afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia, and hypodysfibrinogenemia. Congenital afibrinogenemia is defined...
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disorder is similar to a form of dysfibrinogenemia termed congenital dysfibrinogenemia. However, congenital dysfibrinogenemia differs form hypodysfibrinogenemia...
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cryoglobulinemic disease but are not exacerbated by cold temperature, e.g., dysfibrinogenemia and dysfibrinogenemic disease (conditions involving the intravascular...
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congenital type 3 Dysexecutive syndrome Dysferlinopathy Dysfibrinogenemia, familial Dysfibrinogenemia, acquired Dysgerminoma Dysgraphia Dysharmonic skeletal...
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Hypoprothrombinemia/II Factor VII deficiency Factor X deficiency Factor XII deficiency Factor XIII deficiency Dysfibrinogenemia Congenital afibrinogenemia...
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assays Prolonged Hypo- or afibrinogenemia Fibrinogen quantification Dysfibrinogenemia Fibrinogen activity assay Fibrin(ogen) split products (FSP) FSP or...
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abnormal bleeding and thrombosis but also to cirrhosis. Congenital dysfibrinogenemia, an inherited disorder in which normal levels of fibrinogen composed...
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Protein S deficiency (type I) Factor V Leiden Prothrombin G20210A Dysfibrinogenemia Non O-blood type Low free protein S Activated protein C resistance...
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congenital mutations in the fibrinogen alpha chain and classified as a dysfibrinogenemia (see Hereditary Fibrinogen Aα-Chain Amyloidosis). and, less commonly...
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Leiden and prothrombin G20210A mutations. Blood alterations including dysfibrinogenemia, low free protein S, activated protein C resistance, homocystinuria...
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types. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia and thrombophilia. Alternative splicing of the...
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rare congenital thrombophilias are factor XIII mutation and familial dysfibrinogenemia (an abnormal fibrinogen). It is unclear whether congenital disorders...
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types. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia, afibrinogenemia, and renal amyloidosis. Alternative...
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in this gene lead to several disorders, including afibrinogenemia, dysfibrinogenemia, hypodysfibrinogenemia and thrombotic tendency. Fibrinogen beta chain...
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cryofibrinogenemia but are due to structurally abnormal fibrinogen viz., dysfibrinogenemia and hypodysfibrinogenemia. Based on in vitro studies, three causes...
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S2CID 24223328. Casini A, Neerman-Arbez M, Ariëns RA, de Moerloose P (2015). "Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management"...
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PMID 7112029. Stormorken, H; Brosstad, F; Seim, H (28 April 1983). "A new dysfibrinogenemia: fibrinogen Oslo IV". Thrombosis and Haemostasis. 49 (2): 120–2. PMID 6868008...
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InterPro : Classification of protein families. Retrieved 7 July 2020. Dysfibrinogenemia at eMedicine Borhany, Munira; Pahore, Zaen; ul Qadr, Zeeshan; Rehan...
10 KB (1,134 words) - 14:54, 27 October 2023