Scott syndrome

Scott syndrome is an extremely rare congenital hemorrhagic disorder characterized by hemorrhagic episodes due to impaired platelet coagulant activity.

Also known as: BDPLT7, SCTS, Scott syndrome, prothrombin consumption deficiency, Platelet factor X receptor deficiency, bleeding Abnormality due to deficiency of Platelet binding of Factor 10, bleeding disorder, Platelet-type, 7, prothrombin consumption inhibitor, familial

13 clinical trials for this condition and its sub-types, 0 tagged with Scott syndrome itself.