Thrombotic thrombocytopenic purpura classification: Difference between revisions
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{{Thrombotic thrombocytopenic purpura}} | |||
{{CMG}}; {{AK}} {{S.G.}} | |||
==Overview== | |||
==Classification== | |||
TTP may be classified into several subtypes based on: | |||
#autoantibody against ADAMTS13 | |||
Congenital TTP | |||
Inherited TTP | |||
familial TTP | |||
Upshaw-Schulman syndrome (USS) is an autosomal recessive disease of ADAMTS13 gene on chromosome 9q34 | |||
#gene mutations of ADAMTS13 | |||
==References== | |||
{{Reflist|2}}{{WH}}{{WS}}{{CMG}}{{AE}}{{Saeedeh}} | |||
==Overview== | |||
==References== | |||
{{Reflist|2}} | |||
{{WH}} | |||
{{WS}} | |||
[[Category: (name of the system)]] | |||
* '''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]] | |||
| title = Von Willebrand factor-cleaving protease and Upshaw-Schulman syndrome | |||
| journal = [[International journal of hematology]] | |||
| volume = 75 | |||
| issue = 1 | |||
| pages = 25–34 | |||
| year = 2002 | |||
| month = January | |||
| pmid = 11843286 | |||
}}</ref>. | |||
* '''Acquired:''' Existence of an inhibitory antibody against ADAMS13 due to the variety of conditions. | |||
==References== | |||
{{reflist|2}} | |||
{{WH}} | |||
{{WS}} | |||
[[Category:Disease]] | |||
[[Category:Autoimmune diseases]] | |||
[[Category:Hematology]] | |||
[[Category:Rare diseases]] | |||
[[Category:Dermatology]] | |||
Revision as of 16:58, 12 September 2018
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Thrombotic thrombocytopenic purpura Microchapters |
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Differentiating Thrombotic thrombocytopenic purpura from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Abdurahman Khalil, M.D. [2] Sogand Goudarzi, MD [3]
Overview
Classification
TTP may be classified into several subtypes based on:
- autoantibody against ADAMTS13
Congenital TTP Inherited TTP familial TTP Upshaw-Schulman syndrome (USS) is an autosomal recessive disease of ADAMTS13 gene on chromosome 9q34
- gene mutations of ADAMTS13
References
Template:WHTemplate:WSEditor-In-Chief: C. Michael Gibson, M.S., M.D. [4]Associate Editor(s)-in-Chief: Saeedeh Kowsarnia M.D.[5]
Overview
References
- 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
|month=ignored (help)