| Literature DB >> 19563498 |
A M Mullah-Ali1, A K Chan, D Lillicrap, K Decker, W Seroski, K Moffat, I Walker, M K Pai.
Abstract
von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C). A total absence of FVIII:C has never been reported in type 3 VWD. This case illustrates the effect of severe von Willebrand factor (VWF) deficiency on the factor VIII level.Entities:
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Year: 2009 PMID： 19563498 DOI： 10.1111/j.1365-2516.2009.02062.x
Source DB: PubMed Journal: Haemophilia ISSN： 1351-8216 Impact factor: 4.287