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Medical Term:

congenital afibrinogenemia

 

Definition: a rare disorder of blood coagulation in which little or no fibrinogen can be found in plasma because of a mutant form in one of the three fibrinogen loci. Leads to defective platelet aggregation; autosomal recessive inheritance.

© Copyright 2016 Wolters Kluwer. All Rights Reserved. Review Date: Sep 19, 2016.
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