Churg-Strauss syndrome risk factors: Difference between revisions

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Revision as of 22:39, 30 March 2018

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Overview

There are no established risk factors for [disease name].

OR

The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4].

OR

Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].

OR

Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral.

Risk Factors

There are no established risk factors for [disease name].

OR

The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4].

Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].

Common Risk Factors

Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral.
Common risk factors in the development of [disease name] include:
- [Risk factor 1]
- [Risk factor 2]
- [Risk factor 3]

Less Common Risk Factors

Less common risk factors in the development of [disease name] include:
- [Risk factor 1]
- [Risk factor 2]
- [Risk factor 3]

References

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 __NOTOC__
-{{Churg-Strauss syndrome}}
+{{Xyz}}
-{{CMG}}{{APM}}{{AE}}{{KW}}
+{{CMG}}; {{AE}}
 ==Overview==
-The risk factors associated with Eosinophilic granulomatosis with polyangiitis is not clear. However, various triggering factors have been observed and reported. The risk factors that are likely associated with Eosinophilic granulomatosis with polyangiitis include: infectious agents, drugs, desensitization and or vaccinations.<ref name="pmid24530234">{{cite journal| author=Mouthon L, Dunogue B, Guillevin L| title=Diagnosis and classification of eosinophilic granulomatosis with polyangiitis (formerly named Churg-Strauss syndrome). | journal=J Autoimmun | year= 2014 | volume= 48-49 | issue=  | pages= 99-103 | pmid=24530234 | doi=10.1016/j.jaut.2014.01.018 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24530234  }} </ref>
+There are no established risk factors for [disease name].
+OR
+The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4].
+OR
+Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].
+OR
+Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral.
 ==Risk Factors==
-The risk factors associated with Eosinophilic granulomatosis with polyangiitis is not clear. However, various triggering factors have been observed and reported. The risk factors that are likely associated with Eosinophilic granulomatosis with polyangiitis include: infectious agents, drugs (freebase cocaine<ref name="pmid8834352">{{cite journal| author=Orriols R, Muñoz X, Ferrer J, Huget P, Morell F| title=Cocaine-induced Churg-Strauss vasculitis. | journal=Eur Respir J | year= 1996 | volume= 9 | issue= 1 | pages= 175-7 | pmid=8834352 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8834352  }}</ref>, macrolides<ref name="pmid9555706">{{cite journal| author=Dietz A, Hübner C, Andrassy K| title=[Macrolide antibiotic-induced vasculitis (Churg-Strauss syndrome)]. | journal=Laryngorhinootologie | year= 1998 | volume= 77 | issue= 2 | pages= 111-4 | pmid=9555706 | doi=10.1055/s-2007-996943 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9555706  }}</ref>, carbamazepine<ref name="pmid2918954">{{cite journal| author=Imai H, Nakamoto Y, Hirokawa M, Akihama T, Miura AB| title=Carbamazepine-induced granulomatous necrotizing angiitis with acute renal failure. | journal=Nephron | year= 1989 | volume= 51 | issue= 3 | pages= 405-8 | pmid=2918954 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2918954  }}</ref>, quinine<ref name="pmid2108777">{{cite journal| author=Mathur S, Dooley J, Scheuer PJ| title=Quinine induced granulomatous hepatitis and vasculitis. | journal=BMJ | year= 1990 | volume= 300 | issue= 6724 | pages= 613 | pmid=2108777 | doi= | pmc=1662381 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2108777  }}</ref>), desensitization and or vaccinations.<ref name="pmid24530234" />
+*There are no established risk factors for [disease name].
+OR
+*The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4].
+*Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].
+===Common Risk Factors===
+*Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral.
+*Common risk factors in the development of [disease name] include:
+**[Risk factor 1]
+**[Risk factor 2]
+**[Risk factor 3]
+===Less Common Risk Factors===
+*Less common risk factors in the development of [disease name] include:
+**[Risk factor 1]
+**[Risk factor 2]
+**[Risk factor 3]
 ==References==
 {{Reflist|2}}
-[[Category:Disease]]
-[[Category:Pulmonology]]
-[[Category:Autoimmune diseases]]
-[[Category:Rheumatology]]
-[[Category:Needs content]]
 {{WH}}
 {{WS}}
+[[Category: (name of the system)]]