Congenital fibrinogen disorders with repeated thrombosis
- PMID: 31542854
- DOI: 10.1007/s11239-019-01958-y
Congenital fibrinogen disorders with repeated thrombosis
Abstract
Congenital dysfibrinogenemia is characterized with undetectable or low fibrinogen level by Clauss assay complicated by bleeding and/or thrombosis. These may lead to a diagnostic problem to some clinicians unfamiliar with this disease. We reported a case of congenital dysfibrinogenemia manifested as hemorrhage, repeated thrombosis, low fibrinogen levels through Clauss assay and but normal levels of fibrinogen through PT-derived tests. In conclusion, to patients with thrombosis complicated by decreased fibrinogen level, clinicians and laboratory physicians should be alert to the possibility of congenital dysfibrinogenemia.
Keywords: Congenital dysfibrinogenemia; Congenital fibrinogen disorders; Fibrinogen; Thrombosis.
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