Symptoms mimicking Sjögren syndrome in a heterozygous carrier of CFTR deltaF508 mutation

Pol Arch Med Wewn. 2016 Nov 28;126(11):895-896. doi: 10.20452/pamw.3654. Epub 2016 Nov 28.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Cystic Fibrosis / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • DNA Mutational Analysis
  • Female
  • Heterozygote
  • Humans
  • Middle Aged
  • Mutation*
  • Poland
  • Sjogren's Syndrome / diagnosis*
  • Sjogren's Syndrome / diagnostic imaging
  • Sjogren's Syndrome / genetics

Substances

  • Cystic Fibrosis Transmembrane Conductance Regulator