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| ==Classification==
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| TTP may be classified into several subtypes based on:
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| #autoantibody against ADAMTS13
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| Congenital TTP
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| Inherited TTP
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| familial TTP
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| Upshaw-Schulman syndrome (USS) is an autosomal recessive disease of ADAMTS13 gene on chromosome 9q34
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| #gene mutations of ADAMTS13
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| ==References==
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| {{Reflist|2}}{{WH}}{{WS}}{{CMG}}{{AE}}{{Saeedeh}}
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| ==Overview==
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| ==References==
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| {{Reflist|2}}
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| {{WH}}
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| {{WS}}
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| [[Category: (name of the system)]]
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| * '''Hereditary:'''
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| * Congenital TTP
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| * Inherited TTP
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| * familial TTP
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| * Upshaw-Schulman syndrome (USS) is an autosomal recessive disease of ADAMTS13 gene on chromosome 9q34 <ref>{{Cite journal
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| | author = [[Yoshihiro Fujimura]], [[Masanori Matsumoto]], [[Hideo Yagi]], [[Akira Yoshioka]], [[Taei Matsui]] & [[Koiti Titani]]
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| | title = Von Willebrand factor-cleaving protease and Upshaw-Schulman syndrome
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| | journal = [[International journal of hematology]]
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| | volume = 75
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| | issue = 1
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| | pages = 25–34
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| | year = 2002
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| | month = January
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| | pmid = 11843286
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| }}</ref>.
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| * '''Acquired:''' Existence of an inhibitory antibody against ADAMS13 due to the variety of conditions.
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| ==References==
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| {{reflist|2}}
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| {{WH}}
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| {{WS}}
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| [[Category:Disease]]
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| [[Category:Autoimmune diseases]]
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| [[Category:Hematology]]
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| [[Category:Rare diseases]]
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| [[Category:Dermatology]]
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