Primary ciliary dyskinesia in Amish communities

J Pediatr. 2010 Jun;156(6):1023-1025. doi: 10.1016/j.jpeds.2010.01.054. Epub 2010 Mar 29.

Abstract

Primary ciliary dyskinesia is an autosomal recessive multigenic disease that results in impaired mucociliary clearance. We have diagnosed 9 subjects with primary ciliary dyskinesia from geographically dispersed Amish communities, on the basis of clinical characteristics and ciliary ultrastructural defects. Despite consanguinity, affected individuals had evidence of genetic heterogeneity.

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Christianity
  • Cilia / ultrastructure
  • Ciliary Motility Disorders / epidemiology*
  • Ciliary Motility Disorders / genetics
  • Consanguinity
  • DNA Mutational Analysis
  • Female
  • Humans
  • Infant
  • Male
  • Middle Aged
  • Mucociliary Clearance / genetics
  • Pedigree
  • Young Adult