Mixed connective tissue disease diagnostic study of choice: Difference between revisions
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{{CMG}}; {{AE}} {{SHH}} | {{CMG}}; {{AE}} {{SHH}} | ||
==Overview== | ==Overview== | ||
==Diagnostic Criteria== | ==Diagnostic Criteria== | ||
*The diagnosis of | *The diagnosis of MCTD is made when both of the following diagnostic criteria are met:<ref name="pmid24461387">{{cite journal |vauthors=Tani C, Carli L, Vagnani S, Talarico R, Baldini C, Mosca M, Bombardieri S |title=The diagnosis and classification of mixed connective tissue disease |journal=J. Autoimmun. |volume=48-49 |issue= |pages=46–9 |date=2014 |pmid=24461387 |doi=10.1016/j.jaut.2014.01.008 |url=}}</ref> | ||
**Overlapping clinical features between two or more systemic autoimmune diseases (systemic lupus erythematosus, rheumatoid arthritis, dermatomyositis, polymyositis, and scleroderma) | |||
**Presence of antibodies against the U1 small nuclear ribonucleoprotein autoantigen (U1snRNP) | |||
** | |||
** | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Revision as of 15:29, 3 April 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shaghayegh Habibi, M.D.[2]
Overview
Diagnostic Criteria
- The diagnosis of MCTD is made when both of the following diagnostic criteria are met:[1]
- Overlapping clinical features between two or more systemic autoimmune diseases (systemic lupus erythematosus, rheumatoid arthritis, dermatomyositis, polymyositis, and scleroderma)
- Presence of antibodies against the U1 small nuclear ribonucleoprotein autoantigen (U1snRNP)
References
- ↑ Tani C, Carli L, Vagnani S, Talarico R, Baldini C, Mosca M, Bombardieri S (2014). "The diagnosis and classification of mixed connective tissue disease". J. Autoimmun. 48-49: 46–9. doi:10.1016/j.jaut.2014.01.008. PMID 24461387.