Aims Glanzmann's thrombasthenia is a rare autosomal recessive bleeding disorder of
platelet function caused by a qualitative or quantitative defect of the platelet membrane …

Glanzmann thrombasthenia is an inherited auto-somal recessive disorder characterized by
normal platelet count but lack of platelet aggregation due to absence of platelet glycoprotein …

Glanzmann's thrombasthenia is an autosomal recessive disorder characterized by a lack of
platelet aggregation due to the absence of platelet glycoprotein IIb and IIIa. Usually, the …

Glanzmann's thrombasthenia is a rare inherited bleeding disorder caused by either
quantitative or qualitative abnormalities of the platelet membrane glycoprotein (Gp) IIb/IIIa …

Glanzmann's thrombasthenia (GT) is an autosomal recessive disorder characterized by a
lack of thrombocyte aggregation due to the absence of thrombocyte glycoproteins IIb and …

Glanzmann thrombasthenia is a rare, autosomal recessive, qualitative platelet disorder
resulting from abnormal platelet surface glycoprotein IIb/IIIa. In phenotypically severe cases …

Allogeneic matched bone marrow transplantation (BMT) was performed in a patient with
type I Glanzmann's thrombasthenia, a rare, inherited bleeding disorder caused by a …

Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding disorder
characterized by normal platelet count, but lack of platelet aggregation. The molecular basis …

Glanzmann thrombasthenia (GT) is a rare, autosomal recessive coagulopathy characterized
by either qualitative or quantitative abnormalities of the membrane glycoprotein αIIbβ3 …

Glanzmann thrombasthenia is a rare platelet disorder characterized by an abnormal integrin
receptor on the surface of platelets that results in the failure of platelets to aggregate …