Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria.
Soraya Hadjali-SaichiPhilippe De MazancourtJacqueline Tapon-BretaudièreTristan MiraultKahina GuenounouIssam FrigaaAnne-Marie FischerOuerdia ChafaDominique HelleyPublished in: Haemophilia : the official journal of the World Federation of Hemophilia (2022)
The incidence of afibrinogenemia in Algeria is the consequence of consanguineous marriage in families carrying private mutations. The thrombin generation test (TGT) could identify, among afibrinogenemic patients, those presenting a thrombotic risk.