Die Dysfibrinogenemie is eine autosomal dominante oder rezessive Erkrankung, die durch eine Fehlfunktion des des Fibrinogens hervorgerufen wird. Diese Fehlfunktion kann sich sowohl in einer Hyperkoagulabilität mit Thromboseneigung, wie auch durch eine erhöhte Blutungsbereitsschaft äußern.
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OMIM.ORG article Omim 134820 |