释义 |
Owren disease Ow·ren dis·ease (ō-ren), [MIM*227400] a congenital deficiency of factor V, resulting in prolongation of prothrombin time; bleeding and clotting times are consistently prolonged; autosomal recessive inheritance caused by mutation in the F5 gene on chromosome 1q.Ow·ren dis·ease (ō'ren di-zēz') A congenital deficiency of factor V, resulting in prolongation of prothrombin time; bleeding and clotting times are consistently prolonged; autosomal recessive inheritance caused by mutation in the F5 gene on chromosome 1q. Owren, Paul Arnor, Norwegian hematologist, 1905–. Owren disease - congenital deficiency of factor V, resulting in prolongation of prothrombin time and coagulation time.Ow·ren dis·ease (ō'ren di-zēz') [MIM*227400] A congenital deficiency of factor V, resulting in prolongation of prothrombin time; bleeding and clotting times are consistently prolonged. |