Hereditary platelet function disorders are clinically characterized by recu
rrent surface bleeding and prolonged bleeding time, despite normal platelet
count and coagulation tests. The authors describe persistent thrombopathie
s in two young dogs with increased bleeding tendencies but with normal plas
ma coagulation times and von Willebrand factor (vWf) concentrations. Buccal
mucosal bleeding times were prolonged in both dogs. In aggregation studies
, platelets underwent only a shape change or minimal aggregation in respons
e to adenosine diphosphate and collagen. Whole-platelet adenine nucleotide
concentrations were normal. Electron microscopic evaluation of fibrinogen a
nd vWf binding to the platelets of case no. 1 demonstrated the presence of
glycoprotein Ilb/llla and Ib receptors. Thus, the intrinsic platelet functi
on defects may be different in these two dogs and may likely represent secr
etion/signal transduction disorders.