
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Cryopyrin-associated periodic syndrome causes
Introduction
Overview
Overview
Cryopyrin-associated periodic syndrome is caused by a mutation in the NLRP3, also known as CIAS1, gene.
Causes
Causes
Genetic Causes
References
References
- ↑ Hoffman, Hal M.; Mueller, James L.; Broide, David H.; Wanderer, Alan A.; Kolodner, Richard D. (2001). “Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle–Wells syndrome”. Nature Genetics. 29 (3): 301–305. doi:10.1038/ng756. ISSN 1061-4036.
- ↑ Dodé, Catherine; Le Dû, Nathalie; Cuisset, Laurence; Letourneur, Frank; Berthelot, Jean-Marie; Vaudour, Gérard; Meyrier, Alain; Watts, Richard A; David Scott, G.I.; Nicholls, Anne; Granel, Brigitte; Frances, Camille; Garcier, François; Edery, Patrick; Boulinguez, Serge; Domergues, Jean-Paul; Delpech, Marc; Grateau, Gilles (2002). “New Mutations of CIAS1 That Are Responsible for Muckle-Wells Syndrome and Familial Cold Urticaria: A Novel Mutation Underlies Both Syndromes”. The American Journal of Human Genetics. 70 (6): 1498–1506. doi:10.1086/340786. ISSN 0002-9297.
- ↑ Feldmann, Jérôme; Prieur, Anne-Marie; Quartier, Pierre; Berquin, Patrick; Certain, Stéphanie; Cortis, Elisabetta; Teillac-Hamel, Dominique; Fischer, Alain; Basile, Geneviève de Saint (2002). “Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes”. The American Journal of Human Genetics. 71 (1): 198–203. doi:10.1086/341357. ISSN 0002-9297.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sahar Memar Montazerin, M.D.[2]
