platelet-type von Willebrand disease(English)

• an autosomal dominant bleeding disorder characterized by abnormally enhanced binding of von Willebrand factor by patient platelets. Although the platelet glycoprotein Ib/IX complex is known to constitute the platelet's ristocetin-dependent receptor for VWF, a unique structural abnormality within this complex has only recently been identified
• GP, PRP, PT, RIPA, VWD, VWF
• Hematology, Thrombocyte /thrombosis
• https://doi.org…pnas.88.11.4761