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Annals of Saudi medicine · Jan 2021
Case ReportsVon Willebrand disease type 2B with a novel mutation in the VWF gene.
- Mohammed Abdullah Jeraiby, Susen Sophie, Claudine Caron, Lydia Campos, and Tardy Brigitte.
- From the Department of Pathology, Faculty of Medicine, Jazan University, Prince Muhammed Bin Naser Hospital, Jazan, Saudi Arabia.
- Ann Saudi Med. 2021 Jan 1; 41 (1): 596159-61.
AbstractWe report a 38-year-old woman who presented with a subdural hematoma after minor facial trauma in a stressful situation. The laboratory data showed a subnormal platelet count (166×109/L), VWF:RCo activity was 45% and VWF:Ag was 53% with a VWF:RCo/VWF Ag ratio of 0.79. Hemostasis results and gene analysis revealed von Willebrand disease (VWD) type 2B with normal multimers and a novel mutation c.4136 G>T (R1379L), which appears to be a novel mutation of VWD type 2B that is mainly diagnosed with hypersensitivity to ristocetin and an hyperfixation of platelet Willebrand to a recombinant Gp1b. SIMILAR CASES PUBLISHED: None.
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