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Purtscher-like retinopathy in a patient with Adult-onset Still's disease and concurrent thrombotic thrombocytopenic purpura

✍ Scribed by Okwuosa, Tochi M. ;Lee, Edward W. ;Starosta, Monika ;Chohan, Saima ;Volkov, Suncica ;Flicker, Michael ;Curran, James ;Rezaei, Kourous A. ;Sweiss, Nadera J.

Publisher: John Wiley and Sons
Year: 2007
Tongue: English
Weight: 182 KB
Volume: 57
Category: Article
ISSN: 0004-3591
DOI: 10.1002/art.22477

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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