Thrombotic Thrombocytopenic Purpura, from the Perspectives of a Pediatrician

Title:Thrombotic Thrombocytopenic Purpura, from the Perspectives of a Pediatrician

Volume: 9 Issue: 3

Author(s): Howard H.W. Chan, Anthony K.C. Chan, Iakovina Alexopoulou and Keith K. Lau

Affiliation:

Keywords: Thrombotic thrombocytopenic purpura, hemolytic uremic syndrome, TTP, HUS.

Abstract: Thrombotic thrombocytopenic purpura (TTP) is a rare pediatric disease, yet has grave outcome if not managed properly. It shares many common clinical features with hemolytic uremic syndrome (HUS). While it is still disputable whether TTP and HUS are clinically related disorders, recent studies indicate that severe deficiency of a von Willebrand factor (vWF) cleaving protease is one of the primary causes of TTP. In this discussion, we will focus on TTP in reference to the deficiency of this protease, with the objective of increasing awareness among pediatric healthcare professionals of this less commonly recognized disease.

Cite this article as:

H.W. Chan Howard, K.C. Chan Anthony, Alexopoulou Iakovina and K. Lau Keith, Thrombotic Thrombocytopenic Purpura, from the Perspectives of a Pediatrician, Current Pediatric Reviews 2013; 9 (3) . https://dx.doi.org/10.2174/1573396311309030005

DOI https://dx.doi.org/10.2174/1573396311309030005	Print ISSN 1573-3963
Publisher Name Bentham Science Publisher	Online ISSN 1875-6336