Platelet-type bleeding disorder 16

An inherited blood coagulation disease characterized by autosomal dominant inheritance with macrothrombocytopenia, platelet anisocytosis, prolonged bleeding time but only mildly increased bleeding tendency that has material basis in heterozygous mutation in the ITGA2B gene on chromosome 17q21.31 or the ITGB3 gene on chromosome 17q21.32.

Also known as: bleeding disorder, platelet-type, 16, autosomal dominant, platelet-type bleeding disorder 16, BDPLT16, Glanzmann thrombasthenia, autosomal dominant, bleeding disorder, platelet-type, 16, thrombasthenia of Glanzmann and Naegeli, autosomal dominant

13 clinical trials for this condition and its sub-types, 0 tagged with Platelet-type bleeding disorder 16 itself.