ALB and platelet-type von Willebrand disease: Underlying Coagulopathy was recorded in seven patients and included three cases of haemophilia (two cases of congenital Von Willebrand disease and one case of acquired factor VIII deficiency), one case of thrombocytopenia (PLTs 29 K/μL) and five cases of cirrhosis with severe total protein and albumin deficit (three cases of decompensated cirrhosis).