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Primary ciliary dyskinesia 33

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Description

Primary ciliary dyskinesia-33 is an autosomal recessive disorder characterized by recurrent upper and lower respiratory infections due to defective ciliary clearance and resulting in chronic lung disease. Some patients may have recurrent ear infections resulting in conductive hearing impairment. Examination of respiratory cilia shows subtle movement defects. Laterality defects have not been reported (summary by Olbrich et al., 2015). For a phenotypic description and a discussion of genetic heterogeneity of primary ciliary dyskinesia, see CILD1 (244400).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

93

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Genes

External Links

  • OMIM

    616726

  • Orphanet
  • HPO
  • Medgen

    C4225230

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