Key result
Severe congenital hypofibrinogenemia is linked to recurrent bilateral ischemic necrosis of the digits.
Case Report (n=1)
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Severe hypofibrinogenemia was found in an Algerian woman who, since the age of 37 years, suffered three different episodes of ischemic necrosis of the toes and fingers leading to amputation of the toes and surgical removal of necrotic tissue (necretomy). No anti-fibrinogen antibody was present. The deficiency appeared to be due to severe congenital hypofibrinogenemia since the fibrinogen level remained at the same low level over a long period, without any abnormality of other coagulation proteins. The thrombotic events may be explained by the increased thrombin generation observed in the patient's plasma, due to the lack of thrombin adsorption onto a fibrin net.
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Chafa et al. (1995) conducted a case report in Severe congenital hypofibrinogenemia with bilateral ischemic necrosis of toes and fingers (n=1). Severe congenital hypofibrinogenemia was evaluated on Ischemic necrosis of the toes and fingers. Severe congenital hypofibrinogenemia was associated with 3 episodes of bilateral ischemic necrosis of the toes and fingers in a woman starting at age 37.
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