MOLECULAR ALGORITHM FOR GENETIC DIAGNOSIS OF WOMEN WITH HEMOPHILIA A IN ARGENTINA.

ZIEGLER, BM; ROSSETTI CL; ABELLEYRO, MM; MARCHIONE VD; NEME D; MEDINA-ACOSTA, E; DE BRASI C.D.; RADIC CP

Londres

Congreso; XXX Congress of the International Society on Thrombosis and Haemostasis (ISTH); 2022

BackgroundHemophilia A (HA) is an X-linked recessive bleeding disorder caused by pathogenic variants in FVIII gene (F8), typically expressed in males but rarely in females. Recently a new nomenclature defines Hemophilia carrier women (HC): women/girls with severe, moderate or mild hemophilia (FVIII