Hemolytic-uremic syndrome other diagnostic studies: Difference between revisions
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{{HUS}} | {{HUS}} | ||
{{CMG}} | {{CMG}} {{shyam}}; {{AE}} {{S.G.}} | ||
==Overview== | ==Overview== | ||
Other diagnostic studies associated with HUS include complement protein levels and complement gene mutational analysis. | |||
==Other Diagnostic Studies== | ==Other Diagnostic Studies== | ||
Other diagnostic studies associated with HUS include complement protein levels and complement gene mutational analysis.<ref name="pmid21902819">{{cite journal| author=Loirat C, Frémeaux-Bacchi V| title=Atypical hemolytic uremic syndrome. | journal=Orphanet J Rare Dis | year= 2011 | volume= 6 | issue= | pages= 60 | pmid=21902819 | doi=10.1186/1750-1172-6-60 | pmc=3198674 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21902819 }} </ref> | |||
*Complement factor C3 mutation | |||
*Complement factor C4 mutation | |||
*Complement factor B mutation | |||
*Complement factor H mutation | |||
*Complement factor H-related (CFHR) genes 1-3 mutations | |||
*Complement factor I mutation | |||
*Membrane cofactor protein (MCP) mutation | |||
*Thrombomodulin (THBD) mutation | |||
*Anti-Complement factor H antibody | |||
==References== | ==References== | ||
{{ | {{Reflist|2}} | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
[[Category:Nephrology]] | [[Category:Nephrology]] | ||
[[Category:Hematology]] | [[Category:Hematology]] |
Latest revision as of 02:18, 21 December 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Shyam Patel [2]; Associate Editor(s)-in-Chief: Sogand Goudarzi, MD [3]
Overview
Other diagnostic studies associated with HUS include complement protein levels and complement gene mutational analysis.
Other Diagnostic Studies
Other diagnostic studies associated with HUS include complement protein levels and complement gene mutational analysis.[1]
- Complement factor C3 mutation
- Complement factor C4 mutation
- Complement factor B mutation
- Complement factor H mutation
- Complement factor H-related (CFHR) genes 1-3 mutations
- Complement factor I mutation
- Membrane cofactor protein (MCP) mutation
- Thrombomodulin (THBD) mutation
- Anti-Complement factor H antibody
References
- ↑ Loirat C, Frémeaux-Bacchi V (2011). "Atypical hemolytic uremic syndrome". Orphanet J Rare Dis. 6: 60. doi:10.1186/1750-1172-6-60. PMC 3198674. PMID 21902819.