Thrombotic thrombocytopenic purpura classification: Difference between revisions
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==Overview== | ==Overview== | ||
== Classification == | == Classification == | ||
* '''Hereditary:''' Congenital TTP | * '''Hereditary:''' | ||
* Congenital TTP | |||
* Inherited TTP | |||
* familial TTP | |||
* Upshaw-Schulman syndrome (USS) is an autosomal recessive disease of ADAMTS13 gene on chromosome 9q34 <ref>{{Cite journal | |||
| author = [[Yoshihiro Fujimura]], [[Masanori Matsumoto]], [[Hideo Yagi]], [[Akira Yoshioka]], [[Taei Matsui]] & [[Koiti Titani]] | | author = [[Yoshihiro Fujimura]], [[Masanori Matsumoto]], [[Hideo Yagi]], [[Akira Yoshioka]], [[Taei Matsui]] & [[Koiti Titani]] | ||
| title = Von Willebrand factor-cleaving protease and Upshaw-Schulman syndrome | | title = Von Willebrand factor-cleaving protease and Upshaw-Schulman syndrome |
Revision as of 18:17, 11 September 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Saeedeh Kowsarnia M.D.[2]
Overview
Classification
- Hereditary:
- Congenital TTP
- Inherited TTP
- familial TTP
- Upshaw-Schulman syndrome (USS) is an autosomal recessive disease of ADAMTS13 gene on chromosome 9q34 [1].
- Acquired: Existence of an inhibitory antibody against ADAMS13 due to the variety of conditions.
References
- ↑ Yoshihiro Fujimura, Masanori Matsumoto, Hideo Yagi, Akira Yoshioka, Taei Matsui & Koiti Titani (2002). "Von Willebrand factor-cleaving protease and Upshaw-Schulman syndrome". International journal of hematology. 75 (1): 25–34. PMID 11843286. Unknown parameter
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