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- W1654877604 abstract "Type 2B Von Willebrand disease (vWD) is a rare type of vWD accounting for less than 20 % of the cases of vWD. The characteristic feature of this condition is increased affinity of vWF for the glycoprotein Ib-IX-V complex on platelets resulting in clearing of the high molecular weight vWF multimers and platelets from the circulation. So the patient will present with low levels of vWF as well as thrombocytopenia. This functional abnormality can bedemonstrated by hyperaggregation seen with low dose ristocetin on platelet aggregation. Here we present a case of type 2B vWD in a seven year old male child who presented with skin bleeds and prolonged bleeding following tooth fall. The case is discussed because of its rarity and toemphasize the careful laboratory evaluation required to avoid misdiagnosis in such cases" @default.
- W1654877604 created "2016-06-24" @default.
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- W1654877604 date "2013-01-01" @default.
- W1654877604 modified "2023-09-27" @default.
- W1654877604 title "Von Willebrand disease - Type 2B" @default.
- W1654877604 hasPublicationYear "2013" @default.
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