ERCIYES MEDICAL JOURNAL, cilt.43, sa.2, ss.201-203, 2021 (ESCI)
Background: Type 2B von Willebrand disease (VWD) is a hereditary bleeding disorder caused by changes in the von Willebrand factor (VWF), which increases the binding of VWF to platelets. Type 2B VWD may present with thrombocytopenia.