Inherited Dysfibrinogenemia: Clinical…
Related Articles Inherited dysfibrinogenemia: clinical phenotypes associated with five… more…
Congenital Afibrinogenemia Presenting… ...
Elevated levels of fibrinogen or dysfunctional fibrinogen (dysfibrinogenemia)
Elevated levels of homocysteine
Deficiencies of natural proteins that prevent clotting (such as antithrombin, protein C and protein S)
'Sticky' platelet syndrome ...
The abnormal production of fibrinogen can result in dysfibrinogenemia. The abnormal fibrinogen usually exhibits an abnormal thrombin-mediated conversion to fibrin. ...
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This rare disease is caused by an abnormal gene that must be passed down from both parents. It causes a severe lack of fibrinogen. (Dysfibrinogenemia, in which there is a defect in fibrinogen function, is a different condition.) ...
(AFP) and/or in alkaline phosphatase or a rapid deterioration of hepatic function may be the only clue to the presence of the neoplasm. Infrequently, patients with this disease have polycythemia, hypoglycemia, hypercalcemia, or dysfibrinogenemia.
surgery, heart surgery, or fractures; childbirth within the last 6 months; obesity; and the use of medications such as estrogen and birth control pills, a history of malignant tumor, polycythemia vera, hypercoagulability, or dysfibrinogenemia?
 See also: Surgery, Symptom, Cancer, Death, Prevention
  
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