Rare NLRP12 variants associated with the NLRP12-autoinflammatory disorder phenotype: an Italian case series

Clin Exp Rheumatol. 2013 May-Jun;31(3 Suppl 77):155-6. Epub 2013 Sep 9.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adolescent
  • Adult
  • Child, Preschool
  • Cryopyrin-Associated Periodic Syndromes / drug therapy
  • Cryopyrin-Associated Periodic Syndromes / genetics*
  • Cryopyrin-Associated Periodic Syndromes / immunology
  • Female
  • Genetic Predisposition to Disease
  • Heredity
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Italy
  • Male
  • Middle Aged
  • Mutation*
  • Pedigree
  • Phenotype
  • Treatment Outcome

Substances

  • Immunosuppressive Agents
  • Intracellular Signaling Peptides and Proteins
  • NLRP12 protein, human

Supplementary concepts

  • Familial Cold Autoinflammatory Syndrome 2