Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?

Clin Genet. 2011 Oct;80(4):398-402. doi: 10.1111/j.1399-0004.2010.01620.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Calpain / genetics*
  • Child
  • Child, Preschool
  • Eosinophilia / diagnosis
  • Eosinophilia / genetics*
  • Eosinophils / pathology
  • Female
  • Humans
  • Male
  • Muscle Proteins / genetics*
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • Muscular Dystrophies, Limb-Girdle / diagnosis
  • Muscular Dystrophies, Limb-Girdle / genetics*
  • Mutation*
  • Myositis / diagnosis
  • Myositis / genetics*

Substances

  • Muscle Proteins
  • CAPN3 protein, human
  • Calpain

Supplementary concepts

  • Limb-girdle muscular dystrophy type 2A