Blau Syndrome: A Systemic Granulomatous Disease of Cutaneous Onset and Phenotypic Complexity

Pediatr Dermatol. 2017 Mar;34(2):216-218. doi: 10.1111/pde.13021. Epub 2016 Nov 22.
No abstract available

Publication types

  • Editorial

MeSH terms

  • Arthritis / diagnosis
  • Arthritis / genetics*
  • Humans
  • Mutation
  • Nod2 Signaling Adaptor Protein / genetics*
  • Phenotype
  • Sarcoidosis
  • Synovitis / diagnosis
  • Synovitis / genetics*
  • Uveitis / diagnosis
  • Uveitis / genetics*

Substances

  • NOD2 protein, human
  • Nod2 Signaling Adaptor Protein

Supplementary concepts

  • Blau syndrome