Periodic fever syndrome: Difference between revisions
Jump to navigation
Jump to search
(→Causes) |
No edit summary |
||
Line 17: | Line 17: | ||
*[[Periodic fever, aphthous stomatitis, pharyngitis and adenitis]] ([[Periodic fever, aphthous stomatitis, pharyngitis and adenitis|PFAPA syndrome]]) | *[[Periodic fever, aphthous stomatitis, pharyngitis and adenitis]] ([[Periodic fever, aphthous stomatitis, pharyngitis and adenitis|PFAPA syndrome]]) | ||
*[[Blau syndrome]] | *[[Blau syndrome]] | ||
*[[Pyogenic sterile arthritis, pyoderma gangrenosum, acne]] (PAPA) | *[[Pyogenic sterile arthritis, pyoderma gangrenosum, acne]] ([[PAPA syndrome]]) | ||
==References== | ==References== |
Revision as of 14:15, 5 August 2019
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Autoinflammatory syndrome
Overview
The periodic fever syndromes (also known as autoinflammatory syndromes) are a set of genetic disorders in which the mechanisms which initiate and control inflammation are disturbed leading to uncontrolled inflammation throughout the body. The syndromes are diverse but tend to cause fever, joint pains, abdominal pains and may lead to chronic complications such as amyloidosis.
Causes
- Familial Mediterranean fever
- Hyperimmunoglobulinemia D with recurrent fever
- TNF receptor associated periodic syndrome (TRAPS)
- Cryopyrin-associated periodic syndrome (CAPS) which includes:
- Periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA syndrome)
- Blau syndrome
- Pyogenic sterile arthritis, pyoderma gangrenosum, acne (PAPA syndrome)
References
Stojanov S, Kastner DL. Familial autoinflammatory diseases: genetics, pathogenesis and treatment. Curr Opin Rheumatol. 2005 Sep;17(5):586-99. Review. PMID 16093838