Step 1: Glanzmann thrombasthenia is an autosomal recessive bleeding disorder of platelet function.
Step 2: It is caused by an inherited deficiency or defect of the platelet membrane glycoprotein IIb/IIIa complex (integrin alpha-IIb-beta-3), which is the fibrinogen receptor needed for platelet-to-platelet aggregation. This makes option (b) correct.
Step 3: Because GpIIb/IIIa is absent, primary platelet aggregation with ADP or collagen fails, giving a prolonged bleeding time with a normal platelet count.
Step 4: Decreased GpIb is the defect in Bernard-Soulier syndrome (a), anti-GpIIb/IIIa antibodies cause immune thrombocytopenia (c), and ADAMTS-13 deficiency causes TTP (d) - none of these are Glanzmann thrombasthenia.