Periodic fever syndrome: Difference between revisions
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Stojanov S, Kastner DL. ''Familial autoinflammatory diseases: genetics, pathogenesis and treatment.'' Curr Opin Rheumatol. 2005 Sep;17(5):586-99. Review. PMID 16093838 | Stojanov S, Kastner DL. ''Familial autoinflammatory diseases: genetics, pathogenesis and treatment.'' Curr Opin Rheumatol. 2005 Sep;17(5):586-99. Review. PMID 16093838 | ||
[[Category:Rheumatology]] | [[Category:Rheumatology]] |
Revision as of 14:55, 20 August 2012
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.
Individual periodic fever syndromes
- Familial Mediterranean fever
- Hyperimmunoglobulinemia D with recurrent fever
- TNF receptor associated periodic syndrome (TRAPS)
- Muckle-Wells syndrome
- Familial cold urticaria
- Neonatal onset multisystem inflammatory disease
- Periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA syndrome)
- Blau syndrome
- Pyogenic sterile arthritis, pyoderma gangrenosum, acne (PAPA)
Reference
Stojanov S, Kastner DL. Familial autoinflammatory diseases: genetics, pathogenesis and treatment. Curr Opin Rheumatol. 2005 Sep;17(5):586-99. Review. PMID 16093838