Cystic fibrosis

Am J Clin Pathol. 2003 Dec:120 Suppl:S3-13. doi: 10.1309/DUUVFR11W595V7FE.

Abstract

On a daily basis, pathologists examine the fundamental basis of human diseases using morphologic, immunologic, and molecular techniques. Cystic fibrosis (CF), as a clinically heterogeneous disease, exemplifies the complex challenges of genetic diseases for the pathologist who attempts to explain the mechanisms of disease and provide rationale for clinical management. This review includes an overview of CF and a discussion of pathophysiologic features and practical components of clinical and anatomic pathology, and concludes with a review of molecular diagnostics.

Publication types

  • Review

MeSH terms

  • Bone and Bones / pathology
  • Cystic Fibrosis / diagnosis
  • Cystic Fibrosis / genetics
  • Cystic Fibrosis / pathology*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Humans
  • Liver / pathology
  • Lung / pathology
  • Mutation
  • Pancreas / pathology

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator