platelet-type bleeding disorder 3

A blood platelet disease characterized by enhanced binding of von Willebrand factor by the platelet glycoprotein Ib receptor complex that has_material_basis_in mutation in the GP1BA gene on chromosome 17p13.2.

Signs and symptoms

• Prolonged bleeding time
• Intermittent thrombocytopenia

Also known as: BDPLT3; PT-VWD; platelet type-von Willebrand disease; pseudo-von Willebrand disease; von Willebrand disease platelet-type