Periodic fever syndrome: Difference between revisions
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{{SK}} Autoinflammatory syndrome | {{SK}} Autoinflammatory syndrome | ||
==Overview== | ==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 | 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, [[arthralgia|joint pains]], [[abdominal pain]]s and may lead to chronic complications such as [[amyloidosis]]. | ||
==Causes== | ==Causes== | ||
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*[[Hyperimmunoglobulinemia D with recurrent fever]] | *[[Hyperimmunoglobulinemia D with recurrent fever]] | ||
*[[TNF receptor associated periodic syndrome]] (TRAPS) | *[[TNF receptor associated periodic syndrome]] (TRAPS) | ||
*cryopyrin-associated periodic syndrome (CAPS) | |||
*[[Muckle-Wells syndrome]] | *[[Muckle-Wells syndrome]] | ||
*[[Familial cold urticaria]] | *[[Familial cold urticaria]] |
Revision as of 15:32, 28 June 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)
- 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)
References
Stojanov S, Kastner DL. Familial autoinflammatory diseases: genetics, pathogenesis and treatment. Curr Opin Rheumatol. 2005 Sep;17(5):586-99. Review. PMID 16093838