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Thrombotic thrombocytopenic purpura in a patient with hemoglobin E disease–the importance of timely examination of a blood film

✍ Scribed by Biswadip Hazarika; Barbara J. Bain

Book ID
111994768
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
449 KB
Volume
87
Category
Article
ISSN
0361-8609

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## Abstract Decreased von Willebrand factor (VWF)‐cleaving protease activity (<5%) has been implicated in patients with congenital thrombotic thrombocytopenic purpura–hemolytic uremic syndrome (Upshaw‐Schulman syndrome) and associated with mutations within the __ADAMTS13__ gene. In this report, we