313 top medical experts on Cryopyrin-Associated Periodic Syndromes across 33 countries and 25 U.S. states, including 149 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. 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.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Hereditary Autoinflammatory Diseases (2,464).
  4. Clinical Trials ClinicalTrials.gov : at least 30 including 18 Completed, 6 Recruiting
  5. Synonyms: CINCA Syndrome,  and Articular Syndrome Cutaneous Chronic Infantile Neurological,  Cryopyrin Associated Periodic Syndrome,  Cryopyrinopathy,  Familial Cold Autoinflammatory Syndrome,  Familial Cold Urticaria,  IOMID,  Infantile Onset Multisystem Inflammatory Disease,  Muckle-Wells Syndrome,  Neonatal-Onset Multisystem Inflammatory Disease,  NOMID,  Neonatal Onset Multisystem Inflammatory Disease


  

        

                    


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