Skip to content
2000
Volume 9, Issue 3
  • ISSN: 1573-3963
  • E-ISSN: 1875-6336

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.

Loading

Article metrics loading...

/content/journals/cpr/10.2174/1573396311309030005
2013-08-01
2025-09-11
Loading full text...

Full text loading...

/content/journals/cpr/10.2174/1573396311309030005
Loading

  • Article Type:
    Research Article
Keyword(s): hemolytic uremic syndrome; HUS; Thrombotic thrombocytopenic purpura; TTP
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test