Dysprothrombinaemia is an extremely rare, hereditary disease that has been described in less than 20 families. In contrast to hypoprothrombinaemia, normal concentrations of prothrombin are detectable here, but the activity is extremely weakened.
Dysprothrombinaemia is an extremely rare, hereditary disease that has been described in less than 20 families. In contrast to hypoprothrombinaemia, normal concentrations of prothrombin are detectable here, but the activity is extremely weakened.
The inheritance is autosomal recessive.
Clinically - similar to hypoprothrombinemia - slight bleeding and epistaxis are observed.