Other terms
Cryopyrin associated Periodic Syndromes,Cryopyrin-associated Periodic Syndrome,Periodic Syndrome, Cryopyrin-associated,Periodic Syndromes, Cryopyrin-associated,Syndrome, Cryopyrin-associated Periodic,Syndromes, Cryopyrin-associated Periodic,Cryopyrinopathy,Cryopyrinopathies,Familial Cold Autoinflammatory Syndrome,Familial Cold Urticaria,Cold Urticaria, Familial,Cold Urticarias, Familial,Familial Cold Urticarias,Urticaria, Familial Cold,Urticarias, Familial Cold,Muckle-Wells Syndrome,Muckle Wells Syndrome,Syndrome, Muckle-Wells,Chronic Infantile Neurological, Cutaneous, and Articular Syndrome,Infantile Onset Multisystem Inflammatory Disease,NOMID,Multisystem Inflammatory Disease, Neonatal-Onset,Multisystem Inflammatory Disease, Neonatal Onset,Neonatal Onset Multisystem Inflammatory Disease,CINCA Syndrome,IOMID,IOMIDs
Description
Cryopyrin-associated Periodic Syndromes: A group of rare autosomal dominant diseases, commonly characterized by atypical URTICARIA (hives) with systemic symptoms that develop into end-organ damage. The atypical hives do not involve T-cell or autoantibody. Cryopyrin-associated periodic syndrome includes three previously distinct disorders: Familial cold autoinflammatory syndrome; Muckle-Wells Syndrome; and CINCA Syndrome, that are now considered to represent a disease continuum, all caused by NLRP3 protein mutations.
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