Early lung disease in young children with primary ciliary dyskinesia

David E. Brown, Jessica E. Pittman, Margaret W. Leigh, Lynn Fordham, Stephanie D. Davis

Research output: Contribution to journalArticlepeer-review

54 Scopus citations

Abstract

Primary ciliary dyskinesia (PCD) is an autosomal recessive disease in which ciliary dysfunction leads to chronic lung, sinus, and middle ear disease. PCD is often not diagnosed until late childhood due to its presumed rarity and the technical expertise necessary for diagnosis; as such, little is known about lung disease in young children with PCD. We report on 3 young children with PCD who had evidence of lung disease on infant pulmonary function testing, bronchoscopy, and/or computed tomography (CT) of the chest before 3 years of age.

Original languageEnglish
Pages (from-to)514-516
Number of pages3
JournalPediatric Pulmonology
Volume43
Issue number5
DOIs
StatePublished - May 1 2008
Externally publishedYes

Keywords

  • Bronchiectasis
  • Infant
  • Kartagener syndrome
  • Respiratory function testing
  • Situs inversus

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