European Respiratory Society

Cystic Fibrosis (out of print)

Edited by A.K. Webb and F.A. Ratjen
Cystic Fibrosis (out of print)

This book has been superseded by a newer edition.

When CF was first described the disease was found to be affecting children who died as a result of it within the first few years of their life. However, it became clear that the CF phenotype differs between individuals and this may, in parallel with improved treatment, explain why certain affected individuals appear to have a more beneficial prognosis with prolonged survival. The knowledge regarding CF has increased tremendously. It is now clear that the disease is caused by a mutation in the gene coding for CF transmembrane conductance regulator, an ion channel responsible for chlorine transport in epithelial cells. The treatment has improved substantially and life expectancy has increased from approximately 6 months to 30 yrs. Treatment of airway infections and obstructions, nutritional repletion, anti-inflammatory therapy and lung transplantation have contributed to improve survival outcomes with the possibility of gene therapy soon becoming a probable option. In the present issue of the European Respiratory Monograph, current knowledge regarding CF has been acquired by authors who are true specialists in the field. Most aspects of CF have been covered and this Monograph will be an inestimable source of information for pulmonary physicians and scientists within the field.

  • European Respiratory Society Monographs

Bibliographic Information

Title: 
Cystic Fibrosis (out of print)
Edited by: 
  • A.K. Webb
  • F.A. Ratjen
Published: 
2006-04-01
Copyright year: 
  • 2006
DOI: 
10.1183/1025448x.erm3506
ISBN electronic: 
978-1-904097-85-3
Series: 
European Respiratory Society Monographs
Individual Chapters