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Primary ciliary dyskinesia 32

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Description

Primary ciliary dyskinesia-32 is an autosomal recessive disorder caused by defective structure and function of cilia. Ciliary dysfunction causes respiratory distress in term neonates, impaired mucociliary clearance, chronic respiratory infections, bronchiectasis, and infertility. The ciliary defect affects the central pair complex and radial spokes of the 9+2 motile cilia; affected individuals do not have situs abnormalities (summary by Jeanson et al., 2015). For a general phenotypic description and a discussion of genetic heterogeneity of primary ciliary dyskinesia, see CILD1 (244400).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

84

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Genes

External Links

  • OMIM

    616481

  • Orphanet
  • HPO
  • Medgen

    C4225311

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