A rare cause of hereditary thrombophilia is the genetic variation of the fibrin molecule. This genetic disposition has only been described in about 300 families. Often this mutation is not symptomatic.
DysfibrinogenesisD68.-
DefinitionThis section has been translated automatically.
LiteratureThis section has been translated automatically.
- HA Neumann (2014) The coagulation system. ABW-Wissenschaftsverlag GmbH Berlin S. 232.