Variants
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Primary ciliary dyskinesia 23

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Description

Primary ciliary dyskinesia-23 is an autosomal recessive disorder resulting from defective ciliary motility. Affected individuals have respiratory distress and recurrent upper and lower airway infections, and they often develop bronchiectasis. About 50% of patients have situs inversus or laterality defects. Ultrastructural analysis of respiratory cilia shows defects in the outer dynein arm (summary by Hjeij et al., 2013). For a phenotypic description and a discussion of genetic heterogeneity of primary ciliary dyskinesia, see 244400.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

154

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Genes

External Links

  • OMIM

    615451

  • Orphanet
  • HPO
  • Medgen

    C3809548

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