Congenital factor XI deficiency

Congenital factor XI deficiency is an inherited bleeding disorder characterized by reduced levels and activity of factor XI (FXI) resulting in moderate bleeding symptoms, usually occurring after trauma or surgery.

Also known as: PTA deficiency, Rosenthal factor deficiency, Rosenthal syndrome, Rosenthal's disease, congenital factor XI deficiency, factor XI deficiency, autosomal dominant, factor XI deficiency, autosomal recessive, haemophilia C

13 clinical trials for this condition and its sub-types.