... recognition of the mutated splice site does occur, yielding measurable VWF levels [ 15 ]. To further support this view, homozygotes have greater VWF levels compared to patients with compound heterozygosity for C2362F [ 15 ]. Autosomal recessive disease C2362F Desmopressin response Multimeric patterns...

..., instructions or products referred to in the content or advertisements. Desmopressin response Multimeric patterns Phenotype Platelet adhesion Type 2M von Willebrand disease von Willebrand disease (VWD) is a common, congenital bleeding disorder caused by a deficiency in or dysfunction of von...