血管性血友病因子
血管性血友病
医学
家族史
儿科
免疫学
内科学
血小板
作者
Roy Khalifé,Andrew Aw,Lisa Duffett,Osman Radhwi,Lucie Lacasse,Lothar Huebsch,Mackenzie Bowman,Paula James,Alan Tinmouth
标识
DOI:10.1016/j.clml.2021.01.007
摘要
Acquired von Willebrand syndrome (AVWS) is a bleeding disorder caused by a reduction in the levels and/or activity of von Willebrand factor (VWF) and presents similarly to its inherited alter ego, von Willebrand disease, from a laboratory perspective. AVWS is a rare entity with a reported estimated prevalence of 0.04%, although it may be underreported and often missed.1 The diagnosis of AVWS is based on the new onset of bleeding in an individual who lacks a personal or family bleeding history, laboratory testing compatible with abnormalities in VWF, and the presence of a condition known to cause AVWS.
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