A young Hispanic with c.1646G>A mutation exhibits severe cystic fibrosis lung disease: is ivacaftor an option for therapy?

Am J Respir Crit Care Med. 2012 Oct 1;186(7):694-6. doi: 10.1164/ajrccm.186.7.694.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminophenols / therapeutic use*
  • Child, Preschool
  • Cystic Fibrosis / drug therapy*
  • Cystic Fibrosis / genetics
  • Cystic Fibrosis / pathology
  • Female
  • Hispanic or Latino* / genetics
  • Humans
  • Quinolones / therapeutic use*

Substances

  • Aminophenols
  • Quinolones
  • ivacaftor