Thrombotic thrombocytopenic purpura classification: Difference between revisions
Undo revision 1487789 by Saeedeh Kowsarnia (talk) Tag: Undo |
No edit summary |
||
| Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{Thrombotic thrombocytopenic purpura}} | {{Thrombotic thrombocytopenic purpura}} | ||
{{CMG}} | {{CMG}}{{AE}}{{Saeedeh}} | ||
==Overview== | ==Overview== | ||
== Classification == | == Classification == | ||
Revision as of 16:30, 6 August 2018
|
Thrombotic thrombocytopenic purpura Microchapters |
|
Differentiating Thrombotic thrombocytopenic purpura from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
Thrombotic thrombocytopenic purpura classification On the Web |
|
American Roentgen Ray Society Images of Thrombotic thrombocytopenic purpura classification |
|
Thrombotic thrombocytopenic purpura classification in the news |
|
Directions to Hospitals Treating Thrombotic thrombocytopenic purpura |
|
Risk calculators and risk factors for Thrombotic thrombocytopenic purpura classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Saeedeh Kowsarnia M.D.[2]
Overview
Classification
Roughly, there are two forms of TTP: idiopathic and secondary TTP. A special case is the inherited deficiency of ADAMTS13, known as the Upshaw-Schulman syndrome.